A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698587



Internal ID15435239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61179529..61184733hg38UCSC Ensembl
Innerchr20:59754585..59759789hg19UCSC Ensembl
Innerchr20:59187980..59193184hg18UCSC Ensembl
Innerchr20:59187980..59193184hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385205
hg195205
hg185205
hg175205
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522925
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698587
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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