A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520013



Internal ID15100620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:20684689..20728233hg38UCSC Ensembl
Innerchr1:21011182..21054726hg19UCSC Ensembl
Innerchr1:20883769..20927313hg18UCSC Ensembl
Innerchr1:20756488..20800032hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3843545
hg1943545
hg1843545
hg1743545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697177
Samples
Known GenesKIF17, SH2D5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520013
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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