A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966906



Internal ID18602135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:145996879..145999151hg38UCSC Ensembl
Innerchr7:145693972..145696244hg19UCSC Ensembl
Innerchr7:145324905..145327177hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg382273
hg192273
hg182273
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2486182, nssv2486186, nssv2486177, nssv2486178, nssv2486185, nssv2486184, nssv2486181, nssv2486179, nssv2486180, nssv2486183
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)nsv966906
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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