A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031615



Internal ID19120837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32716562..32735998hg38UCSC Ensembl
Innerchr9:32716560..32735996hg19UCSC Ensembl
Innerchr9:32706560..32725996hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3819437
hg1919437
hg1819437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688866
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031615
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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