A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962872



Internal ID18598114
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761826
SamplesHGDP00927
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962872
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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