A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966897



Internal ID18602126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142450120..142489646hg38UCSC Ensembl
Innerchr7:142142301..142181843hg19UCSC Ensembl
Innerchr7:141818585..141858119hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3839527
hg1939543
hg1839535
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2482417, nssv2482418, nssv2482411, nssv2482415, nssv2482414, nssv2482413, nssv2482410, nssv2482409, nssv2482416, nssv2482412
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)nsv966897
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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