A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761804



Internal ID17757363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1570604..1620470hg38UCSC Ensembl
Innerchr20:1551250..1601116hg19UCSC Ensembl
Innerchr20:1499250..1549116hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3849867
hg1949867
hg1849867
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv965840
Supporting Variants
SamplesHGDP00521
Known GenesSIRPB1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761804
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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