A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526087



Internal ID15453380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:57110765..57113937hg38UCSC Ensembl
Innerchr1:57576438..57579610hg19UCSC Ensembl
Innerchr1:57349026..57352198hg18UCSC Ensembl
Innerchr1:57288459..57291631hg17UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg383173
hg193173
hg183173
hg173173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702333
Samples
Known GenesDAB1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526087
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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