A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690614



Internal ID18988895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13723813..13760987hg38UCSC Ensembl
Innerchr9:13723812..13760986hg19UCSC Ensembl
Innerchr9:13713812..13750986hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3837175
hg1937175
hg1837175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032702
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)nssv3690614
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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