A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2764540



Internal ID17822429
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv981349
Supporting Variants
SamplesHGDP00927
Known GenesDUSP22
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2764540
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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