A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695171



Internal ID18646766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116677781..116825537hg38UCSC Ensembl
Innerchr9:119440060..119587816hg19UCSC Ensembl
Innerchr9:118479881..118627637hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38147757
hg19147757
hg18147757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043149
Supporting Variants
Samples
Known GenesASTN2, TRIM32
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695171
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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