A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690632



Internal ID18988913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15845904..15878117hg38UCSC Ensembl
Innerchr9:15845902..15878115hg19UCSC Ensembl
Innerchr9:15835902..15868115hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3832214
hg1932214
hg1832214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032081
Supporting Variants
Samples
Known GenesCCDC171
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690632
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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