A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437548



Internal ID15382854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54121396..54121643hg38UCSC Ensembl
Outerchr7:54109419..54129355hg38UCSC Ensembl
Innerchr7:54189089..54189336hg19UCSC Ensembl
Outerchr7:54177112..54197048hg19UCSC Ensembl
Innerchr7:54156583..54156830hg18UCSC Ensembl
Outerchr7:54144606..54164542hg18UCSC Ensembl
Innerchr7:53930838..53931085hg16UCSC Ensembl
Outerchr7:53918861..53938797hg16UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3819937
hg1919937
hg1819937
hg1619937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467429
SamplesNA19208
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)nsv437548
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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