A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963349



Internal ID18598590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103240913..103241413hg38UCSC Ensembl
Innerchr3:102959757..102960257hg19UCSC Ensembl
Innerchr3:104442447..104442947hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2292827, nssv2292821, nssv2292826, nssv2292823, nssv2292828, nssv2292822, nssv2292824, nssv2292829, nssv2292820, nssv2292825
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)nsv963349
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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