A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966908



Internal ID18602137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149671401..149687858hg38UCSC Ensembl
Innerchr7:149368492..149384949hg19UCSC Ensembl
Innerchr7:148999425..149015882hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3816458
hg1916458
hg1816458
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2485454, nssv2485460, nssv2485455, nssv2485459, nssv2485456, nssv2485451, nssv2485452, nssv2485453, nssv2485457, nssv2485458
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)nsv966908
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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