A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702122



Internal ID15438774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61228576..61233003hg38UCSC Ensembl
Innerchr20:59803632..59808059hg19UCSC Ensembl
Innerchr20:59237027..59241454hg18UCSC Ensembl
Innerchr20:59237027..59241454hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384428
hg194428
hg184428
hg174428
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525918
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702122
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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