A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437579



Internal ID15382885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:163440411..163443517hg38UCSC Ensembl
Outerchr2:163439426..163452457hg38UCSC Ensembl
Innerchr2:164296921..164300027hg19UCSC Ensembl
Outerchr2:164295936..164308967hg19UCSC Ensembl
Innerchr2:164005167..164008273hg18UCSC Ensembl
Outerchr2:164004182..164017213hg18UCSC Ensembl
Innerchr2:164499465..164502571hg16UCSC Ensembl
Outerchr2:164498480..164511511hg16UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3813032
hg1913032
hg1813032
hg1613032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467460
SamplesNA07048
Known Genes
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv437579
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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