A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515702



Internal ID15443313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:99211270..99306504hg38UCSC Ensembl
Innerchr2:99827733..99922967hg19UCSC Ensembl
Innerchr2:99194165..99289399hg18UCSC Ensembl
Innerchr2:99286251..99381485hg17UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3895235
hg1995235
hg1895235
hg1795235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668274, nssv677899, nssv664473, nssv671985
Samples
Known GenesLYG1, LYG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515702
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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