A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690627



Internal ID18988908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15565672..15595593hg38UCSC Ensembl
Innerchr9:15565670..15595591hg19UCSC Ensembl
Innerchr9:15555670..15585591hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3829922
hg1929922
hg1829922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034795
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)nssv3690627
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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