A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702572



Internal ID15439224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:80446161..80455103hg38UCSC Ensembl
Innerchr17:78419961..78428903hg19UCSC Ensembl
Innerchr17:76034556..76043498hg18UCSC Ensembl
Innerchr17:76034556..76043498hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg388943
hg198943
hg188943
hg178943
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526291
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702572
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