A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611020



Internal ID16398429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39381083..39529660hg38UCSC Ensembl
Innerchr8:39238602..39387179hg19UCSC Ensembl
Innerchr8:39357759..39506336hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38148578
hg19148578
hg18148578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12095n54
Supporting Variantsnssv1111101
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611020
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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