A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979824



Internal ID18268339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:43037611..43038712hg38UCSC Ensembl
Innerchr3:43079103..43080204hg19UCSC Ensembl
Innerchr3:43054107..43055208hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg381102
hg191102
hg181102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2278995, nssv2278988, nssv2278991, nssv2278994, nssv2278996, nssv2278993, nssv2278992, nssv2278997, nssv2278990, nssv2278989
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFAM198A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979824
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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