A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528707



Internal ID15109314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:111919015..111920819hg38UCSC Ensembl
Innerchr1:112461637..112463441hg19UCSC Ensembl
Innerchr1:112263160..112264964hg18UCSC Ensembl
Innerchr1:112173679..112175483hg17UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381805
hg191805
hg181805
hg171805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705354
Samples
Known GenesKCND3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528707
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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