A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669600



Internal ID15406252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57395277..57421679hg38UCSC Ensembl
Innerchr20:55970333..55996735hg19UCSC Ensembl
Innerchr20:55403739..55430141hg18UCSC Ensembl
Innerchr20:55403739..55430141hg17UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3826403
hg1926403
hg1826403
hg1726403
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516617
Supporting Variants
Samples
Known GenesMIR5095, RBM38
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669600
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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