A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963392



Internal ID18598633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:190876522..190878282hg38UCSC Ensembl
Innerchr3:190594311..190596071hg19UCSC Ensembl
Innerchr3:192077005..192078765hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381761
hg191761
hg181761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2312167, nssv2312166, nssv2312168, nssv2312164, nssv2312163, nssv2312165, nssv2312161, nssv2312162, nssv2312160, nssv2312169
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSNAR-I
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963392
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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