A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611032



Internal ID16398441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39393511..39532700hg38UCSC Ensembl
Innerchr8:39251030..39390219hg19UCSC Ensembl
Innerchr8:39370187..39509376hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38139190
hg19139190
hg18139190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12095n54
Supporting Variantsnssv1111144, nssv1111145
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611032
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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