A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522156



Internal ID15102763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101844093..101956158hg38UCSC Ensembl
Innerchr1:102309649..102421714hg19UCSC Ensembl
Innerchr1:102082237..102194302hg18UCSC Ensembl
Innerchr1:102021670..102133735hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38112066
hg19112066
hg18112066
hg17112066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694929
Samples
Known GenesDNAJA1P5, MIR548AI, OLFM3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522156
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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