A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761088



Internal ID17858021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17558872..17568045hg38UCSC Ensembl
Innerchr21:18931190..18940363hg19UCSC Ensembl
Innerchr21:17853061..17862234hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg389174
hg199174
hg189174
Variant TypeCNV duplication
Copy Number5
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv966035
Supporting Variants
SamplesHGDP01029
Known GenesCXADR
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761088
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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