A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690609



Internal ID18988890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13308617..13340591hg38UCSC Ensembl
Innerchr9:13308616..13340590hg19UCSC Ensembl
Innerchr9:13298616..13330590hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3831975
hg1931975
hg1831975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015235
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)nssv3690609
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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