A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981603



Internal ID18616800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:145036713..145041137hg38UCSC Ensembl
Innerchr7:144733806..144738230hg19UCSC Ensembl
Innerchr7:144364739..144369163hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg384425
hg194425
hg184425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2485130, nssv2485128, nssv2485134, nssv2485126, nssv2485133, nssv2485129, nssv2485127, nssv2485132, nssv2485125, nssv2485131
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)nsv981603
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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