A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963352



Internal ID18598593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:117026696..117034955hg38UCSC Ensembl
Innerchr3:116745543..116753802hg19UCSC Ensembl
Innerchr3:118228233..118236492hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg388260
hg198260
hg188260
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2293652, nssv2293648, nssv2293645, nssv2293650, nssv2293644, nssv2293653, nssv2293649, nssv2293647, nssv2293651, nssv2293646
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)nsv963352
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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