A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704082



Internal ID15440734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15574855..15579746hg38UCSC Ensembl
Innerchr9:15574853..15579744hg19UCSC Ensembl
Innerchr9:15564853..15569744hg18UCSC Ensembl
Innerchr9:15564853..15569744hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg384892
hg194892
hg184892
hg174892
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527616
Supporting Variants
Samples
Known GenesCCDC171
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704082
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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