A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970175



Internal ID18605399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149965525..149979101hg38UCSC Ensembl
Innerchr6:150286661..150300237hg19UCSC Ensembl
Innerchr6:150328354..150341930hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3813577
hg1913577
hg1813577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2428439, nssv2428448, nssv2428443, nssv2428440, nssv2428447, nssv2428444, nssv2428441, nssv2428446, nssv2428442, nssv2428445
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesULBP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970175
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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