A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523855



Internal ID15451148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61418877..61439473hg38UCSC Ensembl
Innerchr17:59496238..59516834hg19UCSC Ensembl
Innerchr17:56851020..56871616hg18UCSC Ensembl
Innerchr17:56851020..56871616hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3820597
hg1920597
hg1820597
hg1720597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699690
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523855
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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