A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526371



Internal ID15106978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6247195..6307159hg38UCSC Ensembl
Innerchr1:6307255..6367219hg19UCSC Ensembl
Innerchr1:6229842..6289806hg18UCSC Ensembl
Innerchr1:6241521..6301485hg17UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3859965
hg1959965
hg1859965
hg1759965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702667
Samples
Known GenesACOT7, GPR153
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526371
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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