A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654412



Internal ID15044378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:149494291..149522775hg38UCSC Ensembl
Innerchr5:148873854..148902338hg19UCSC Ensembl
Innerchr5:148854047..148882531hg18UCSC Ensembl
Innerchr5:148854047..148882531hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3828485
hg1928485
hg1828485
hg1728485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516848
Supporting Variants
Samples
Known GenesCSNK1A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654412
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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