A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979826



Internal ID18268341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44872532..44874641hg38UCSC Ensembl
Innerchr3:44914024..44916133hg19UCSC Ensembl
Innerchr3:44889028..44891137hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382110
hg192110
hg182110
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2280046, nssv2280050, nssv2280052, nssv2280048, nssv2280053, nssv2280047, nssv2280044, nssv2280049, nssv2280045, nssv2280051
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTGM4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979826
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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