A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524189



Internal ID15451482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:43738398..43743718hg38UCSC Ensembl
Innerchr17:41815766..41821086hg19UCSC Ensembl
Innerchr17:39171292..39176612hg18UCSC Ensembl
Innerchr17:39171292..39176612hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg385321
hg195321
hg185321
hg175321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700072
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524189
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