A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022632



Internal ID19111850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32087211..32211780hg38UCSC Ensembl
Innerchr9:32087209..32211778hg19UCSC Ensembl
Innerchr9:32077209..32201778hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38124570
hg19124570
hg18124570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7514n100
Supporting Variantsnssv3688862, nssv3688863
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)nsv1022632
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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