A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687866



Internal ID15424518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69228706..69230502hg38UCSC Ensembl
Innerchr17:67224847..67226643hg19UCSC Ensembl
Innerchr17:64736442..64738238hg18UCSC Ensembl
Innerchr17:64736442..64738238hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381797
hg191797
hg181797
hg171797
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)nssv687866
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer