A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970114



Internal ID18258652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:43308759..43313415hg38UCSC Ensembl
Innerchr6:43276497..43281153hg19UCSC Ensembl
Innerchr6:43384475..43389131hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg384657
hg194657
hg184657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2408151, nssv2408145, nssv2408144, nssv2408150, nssv2408143, nssv2408147, nssv2408149, nssv2408142, nssv2408146, nssv2408148
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesCRIP3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970114
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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