A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966891



Internal ID18602120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:136258223..136265012hg38UCSC Ensembl
Innerchr7:135942971..135949760hg19UCSC Ensembl
Innerchr7:135593511..135600300hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg386790
hg196790
hg186790
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2480001, nssv2480002, nssv2479999, nssv2479994, nssv2479997, nssv2479993, nssv2479998, nssv2480000, nssv2479996, nssv2479995
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)nsv966891
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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