A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527862



Internal ID15108469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178537459..178582337hg38UCSC Ensembl
Innerchr1:178506594..178551472hg19UCSC Ensembl
Innerchr1:176773217..176818095hg18UCSC Ensembl
Innerchr1:175238251..175283129hg17UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3844879
hg1944879
hg1844879
hg1744879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704360
Samples
Known GenesC1orf220
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527862
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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