A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690613



Internal ID18988894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13669863..13756711hg38UCSC Ensembl
Innerchr9:13669862..13756710hg19UCSC Ensembl
Innerchr9:13659862..13746710hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3886849
hg1986849
hg1886849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018933
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)nssv3690613
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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