A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695199



Internal ID18993480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116810790..116843139hg38UCSC Ensembl
Innerchr9:119573069..119605418hg19UCSC Ensembl
Innerchr9:118612890..118645239hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3832350
hg1932350
hg1832350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047370
Supporting Variants
Samples
Known GenesASTN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695199
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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