A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696252



Internal ID18647847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69482727..69498585hg38UCSC Ensembl
Innerchr9:72097643..72113501hg19UCSC Ensembl
Innerchr9:71287463..71303321hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3815859
hg1915859
hg1815859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047120
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)nssv3696252
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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