A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611017



Internal ID16398426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380500..39386523hg38UCSC Ensembl
Innerchr8:39238019..39244042hg19UCSC Ensembl
Innerchr8:39357176..39363199hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg386024
hg196024
hg186024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12101n54
Supporting Variantsnssv1111098
Samples
Known GenesADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611017
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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