A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696163



Internal ID18994444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64683555..64930080hg38UCSC Ensembl
Innerchr9:69695973..69942498hg19UCSC Ensembl
Innerchr9:68985793..69232318hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38246526
hg19246526
hg18246526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030830
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696163
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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