A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966885



Internal ID18602114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128572761..128616246hg38UCSC Ensembl
Innerchr7:128212815..128256300hg19UCSC Ensembl
Innerchr7:128000051..128043536hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3843486
hg1943486
hg1843486
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2477092, nssv2477094, nssv2477098, nssv2477091, nssv2477100, nssv2477099, nssv2477097, nssv2477096, nssv2477095, nssv2477093
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)nsv966885
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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