A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969404



Internal ID18257945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57436476..60411559hg38UCSC Ensembl
Innerchr6:57301274..57383601hg19UCSC Ensembl
Innerchr6:57409233..57491560hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg382975084
hg1982328
hg1882328
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2409962, nssv2409967, nssv2409960, nssv2409966, nssv2409964, nssv2409958, nssv2409963, nssv2409965, nssv2409959, nssv2409961
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesPRIM2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969404
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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