A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698440



Internal ID15435092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:20668459..20676233hg38UCSC Ensembl
Innerchr1:20994952..21002726hg19UCSC Ensembl
Innerchr1:20867539..20875313hg18UCSC Ensembl
Innerchr1:20740258..20748032hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg387775
hg197775
hg187775
hg177775
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522796
Supporting Variants
Samples
Known GenesKIF17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698440
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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