A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437463



Internal ID15382769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:39816019..39816197hg38UCSC Ensembl
Outerchr5:39806062..39829762hg38UCSC Ensembl
Innerchr5:39816121..39816299hg19UCSC Ensembl
Outerchr5:39806164..39829864hg19UCSC Ensembl
Innerchr5:39851878..39852056hg18UCSC Ensembl
Outerchr5:39841921..39865621hg18UCSC Ensembl
Innerchr5:39861622..39861800hg16UCSC Ensembl
Outerchr5:39851665..39875365hg16UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3823701
hg1923701
hg1823701
hg1623701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467344
SamplesNA18521
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)nsv437463
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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