A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522805



Internal ID15103412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:26671721..26705943hg38UCSC Ensembl
Innerchr2:26894589..26928811hg19UCSC Ensembl
Innerchr2:26748093..26782315hg18UCSC Ensembl
Innerchr2:26806240..26840462hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3834223
hg1934223
hg1834223
hg1734223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698450
Samples
Known GenesKCNK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522805
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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