A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660982



Internal ID15397634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:117437210..117472285hg38UCSC Ensembl
Innerchr1:117979832..118014907hg19UCSC Ensembl
Innerchr1:117781355..117816430hg18UCSC Ensembl
Innerchr1:117691874..117726949hg17UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3835076
hg1935076
hg1835076
hg1735076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519780
Supporting Variants
Samples
Known GenesMAN1A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660982
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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