A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612872



Internal ID16400281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143618822..143631117hg38UCSC Ensembl
Innerchr8:144700992..144713287hg19UCSC Ensembl
Innerchr8:144772135..144784430hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3812296
hg1912296
hg1812296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12427n54
Supporting Variantsnssv1125694
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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