A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671444



Internal ID15061410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14878264..14947216hg38UCSC Ensembl
Innerchr20:14858910..14927862hg19UCSC Ensembl
Innerchr20:14806910..14875862hg18UCSC Ensembl
Innerchr20:14806910..14875862hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3868953
hg1968953
hg1868953
hg1768953
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520440
Supporting Variants
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671444
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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