A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705354



Internal ID15095320
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528707
Supporting Variants
Samples
Known GenesKCND3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705354
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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