A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696251



Internal ID18647846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69475890..69505349hg38UCSC Ensembl
Innerchr9:72090806..72120265hg19UCSC Ensembl
Innerchr9:71280626..71310085hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3829460
hg1929460
hg1829460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035814
Supporting Variants
Samples
Known GenesAPBA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696251
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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