A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522589



Internal ID15449882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:7447582..7459204hg38UCSC Ensembl
Innerchr1:7507642..7519264hg19UCSC Ensembl
Innerchr1:7430229..7441851hg18UCSC Ensembl
Innerchr1:7441908..7453530hg17UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3811623
hg1911623
hg1811623
hg1711623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705976
Samples
Known GenesCAMTA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522589
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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