A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521025



Internal ID15101632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20294711..20611608hg38UCSC Ensembl
Innerchr17:20198024..20514921hg19UCSC Ensembl
Innerchr17:20138616..20455513hg18UCSC Ensembl
Innerchr17:20138616..20455513hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38316898
hg19316898
hg18316898
hg17316898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697741
Samples
Known GenesCCDC144CP, CDRT15L2, KRT16P3, LGALS9B, SPECC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521025
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