A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523435



Internal ID15104042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:26648365..26705943hg38UCSC Ensembl
Innerchr2:26871233..26928811hg19UCSC Ensembl
Innerchr2:26724737..26782315hg18UCSC Ensembl
Innerchr2:26782884..26840462hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3857579
hg1957579
hg1857579
hg1757579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699190
Samples
Known GenesKCNK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523435
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