A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526148



Internal ID15453441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:55635924..55680777hg38UCSC Ensembl
Innerchr1:56101597..56146450hg19UCSC Ensembl
Innerchr1:55874185..55919038hg18UCSC Ensembl
Innerchr1:55813618..55858471hg17UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3844854
hg1944854
hg1844854
hg1744854
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702406
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526148
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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