A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516343



Internal ID15443636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37381254..37447464hg38UCSC Ensembl
Innerchr20:36009657..36075866hg19UCSC Ensembl
Innerchr20:35443071..35509280hg18UCSC Ensembl
Innerchr20:35443071..35509280hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3866211
hg1966210
hg1866210
hg1766210
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703703, nssv667711, nssv686877, nssv696467, nssv680916, nssv673589, nssv699382, nssv663705, nssv658052
Samples
Known GenesSRC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516343
Frequency
Sample Size2026
Observed Gain1
Observed Loss8
Observed Complex0
Frequencyn/a


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