A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670999



Internal ID15407651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69214126..69233646hg38UCSC Ensembl
Innerchr17:67210267..67229787hg19UCSC Ensembl
Innerchr17:64721862..64741382hg18UCSC Ensembl
Innerchr17:64721862..64741382hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3819521
hg1919521
hg1819521
hg1719521
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516799
Supporting Variants
Samples
Known GenesABCA10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670999
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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