A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981349



Internal ID18616547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:256049..296767hg38UCSC Ensembl
Innerchr6:256049..296767hg19UCSC Ensembl
Innerchr6:201049..241767hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3840719
hg1940719
hg1840719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764540, nssv2765242, nssv2762051, nssv2762816, nssv2764415, nssv2758501
SamplesHGDP01284, HGDP00778, HGDP01307, HGDP01029, HGDP00456, HGDP00927
Known GenesDUSP22
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981349
Frequency
Sample Size10
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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