A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690604



Internal ID18988885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13307704..13340012hg38UCSC Ensembl
Innerchr9:13307703..13340011hg19UCSC Ensembl
Innerchr9:13297703..13330011hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3832309
hg1932309
hg1832309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028113
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)nssv3690604
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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