A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611077



Internal ID16398486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39487454..39529660hg38UCSC Ensembl
Innerchr8:39344973..39387179hg19UCSC Ensembl
Innerchr8:39464130..39506336hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3842207
hg1942207
hg1842207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12110n54
Supporting Variantsnssv1111243
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611077
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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