A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699925



Internal ID15089891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37248607..37466486hg38UCSC Ensembl
Innerchr20:35877010..36094888hg19UCSC Ensembl
Innerchr20:35310424..35528302hg18UCSC Ensembl
Innerchr20:35310424..35528302hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38217880
hg19217879
hg18217879
hg17217879
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524059
Supporting Variants
Samples
Known GenesGHRH, MANBAL, SRC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699925
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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