A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696244



Internal ID18647839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69417465..69454398hg38UCSC Ensembl
Innerchr9:72032381..72069314hg19UCSC Ensembl
Innerchr9:71222201..71259134hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3836934
hg1936934
hg1836934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041436
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)nssv3696244
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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