A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761826



Internal ID17824119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47822798..47840761hg38UCSC Ensembl
Innerchr22:48218547..48236510hg19UCSC Ensembl
Innerchr22:46597211..46615174hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3817964
hg1917964
hg1817964
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv962872
Supporting Variants
SamplesHGDP00927
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761826
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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