A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966838



Internal ID18602067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67083089..67152516hg38UCSC Ensembl
Innerchr7:66548076..66617503hg19UCSC Ensembl
Innerchr7:66185511..66254938hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3869428
hg1969428
hg1869428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2459858, nssv2459853, nssv2459856, nssv2459855, nssv2459854, nssv2459859, nssv2459857, nssv2459852, nssv2459851, nssv2459850
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR4650-1, MIR4650-2, TYW1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966838
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