A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696467



Internal ID15433119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37381254..37435163hg38UCSC Ensembl
Innerchr20:36009657..36063565hg19UCSC Ensembl
Innerchr20:35443071..35496979hg18UCSC Ensembl
Innerchr20:35443071..35496979hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3853910
hg1953909
hg1853909
hg1753909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516343
Supporting Variants
Samples
Known GenesSRC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696467
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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