A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043149



Internal ID18785680
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 StatusM
Merged Variants
Supporting Variantsnssv3695171
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)nsv1043149
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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