A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981919



Internal ID18617115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23203477..23212281hg38UCSC Ensembl
Innerchr8:23060990..23069794hg19UCSC Ensembl
Innerchr8:23116935..23125739hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg388805
hg198805
hg188805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2497666, nssv2497663, nssv2497668, nssv2497670, nssv2497667, nssv2497665, nssv2497661, nssv2497669, nssv2497662, nssv2497664
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTNFRSF10A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981919
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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