A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690617



Internal ID18988898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13861067..13923674hg38UCSC Ensembl
Innerchr9:13861066..13923673hg19UCSC Ensembl
Innerchr9:13851066..13913673hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3862608
hg1962608
hg1862608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032447
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)nssv3690617
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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