A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527595



Internal ID15454888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:7497092..7507352hg38UCSC Ensembl
Innerchr1:7557152..7567412hg19UCSC Ensembl
Innerchr1:7479739..7489999hg18UCSC Ensembl
Innerchr1:7491418..7501678hg17UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3810261
hg1910261
hg1810261
hg1710261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704056
Samples
Known GenesCAMTA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527595
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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