A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523989



Internal ID15104596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6351154..6396412hg38UCSC Ensembl
Innerchr1:6411214..6456472hg19UCSC Ensembl
Innerchr1:6333801..6379059hg18UCSC Ensembl
Innerchr1:6345480..6390738hg17UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3845259
hg1945259
hg1845259
hg1745259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699845
Samples
Known GenesACOT7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523989
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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