A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981183



Internal ID18616382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:128638275..128640301hg38UCSC Ensembl
Innerchr6:128959420..128961446hg19UCSC Ensembl
Innerchr6:129001113..129003139hg18UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg382027
hg192027
hg182027
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2422222, nssv2422220, nssv2422218, nssv2422215, nssv2422214, nssv2422216, nssv2422219, nssv2422221, nssv2422213, nssv2422217
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981183
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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