A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963299



Internal ID18598540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14194919..14198307hg38UCSC Ensembl
Innerchr3:14236419..14239807hg19UCSC Ensembl
Innerchr3:14211423..14214811hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg383389
hg193389
hg183389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2274521, nssv2274520, nssv2274519, nssv2274522, nssv2274524, nssv2274523, nssv2274527, nssv2274526, nssv2274525, nssv2274518
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLSM3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963299
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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