A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696131



Internal ID18994412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64462496..64886202hg38UCSC Ensembl
Innerchr9:69474914..69898620hg19UCSC Ensembl
Innerchr9:68764734..69188440hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38423707
hg19423707
hg18423707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021051
Supporting Variants
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696131
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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