A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611024



Internal ID16398433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39386829..39529660hg38UCSC Ensembl
Innerchr8:39244348..39387179hg19UCSC Ensembl
Innerchr8:39363505..39506336hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38142832
hg19142832
hg18142832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12093n54
Supporting Variantsnssv1111105, nssv1111106
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611024
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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