A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704190



Internal ID15440842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3862380..3870321hg38UCSC Ensembl
Innerchr20:3843027..3850968hg19UCSC Ensembl
Innerchr20:3791027..3798968hg18UCSC Ensembl
Innerchr20:3791027..3798968hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387942
hg197942
hg187942
hg177942
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527710
Supporting Variants
Samples
Known GenesMAVS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704190
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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