A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965221



Internal ID18600455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149462520..149464121hg38UCSC Ensembl
Innerchr3:149180307..149181908hg19UCSC Ensembl
Innerchr3:150662997..150664598hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381602
hg191602
hg181602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2300970, nssv2300973, nssv2300969, nssv2300972, nssv2300968, nssv2300966, nssv2300971, nssv2300967, nssv2300965, nssv2300964
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)nsv965221
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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