A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965783



Internal ID18601013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160734836..160735833hg38UCSC Ensembl
Innerchr6:161155868..161156865hg19UCSC Ensembl
Innerchr6:161075858..161076855hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38998
hg19998
hg18998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2429656, nssv2429655, nssv2429663, nssv2429657, nssv2429660, nssv2429662, nssv2429661, nssv2429654, nssv2429658, nssv2429659
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPLG
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965783
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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