A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970868



Internal ID18606090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66570232..66591623hg38UCSC Ensembl
Innerchr7:66035219..66056610hg19UCSC Ensembl
Innerchr7:65672654..65694045hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3821392
hg1921392
hg1821392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2459443, nssv2459447, nssv2459444, nssv2459445, nssv2459448, nssv2459439, nssv2459442, nssv2459446, nssv2459441, nssv2459440
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC493754
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970868
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer