A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963373



Internal ID18598614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:160567953..160569320hg38UCSC Ensembl
Innerchr3:160285741..160287108hg19UCSC Ensembl
Innerchr3:161768435..161769802hg18UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg381368
hg191368
hg181368
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2303522, nssv2303524, nssv2303520, nssv2303517, nssv2303518, nssv2303519, nssv2303521, nssv2303523, nssv2303516, nssv2303525
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)nsv963373
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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