A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2756979



Internal ID17737135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:18979534..18985958hg38UCSC Ensembl
Innerchr20:18960178..18966602hg19UCSC Ensembl
Innerchr20:18908178..18914602hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg386425
hg196425
hg186425
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv965934
Supporting Variants
SamplesHGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2756979
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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