A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700983



Internal ID15090949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64141284..64247978hg38UCSC Ensembl
Innerchr20:62772637..62879331hg19UCSC Ensembl
Innerchr20:62243081..62349775hg18UCSC Ensembl
Innerchr20:62243081..62349775hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38106695
hg19106695
hg18106695
hg17106695
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524962
Supporting Variants
Samples
Known GenesMYT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700983
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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