A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970156



Internal ID18605380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:105081780..105083349hg38UCSC Ensembl
Innerchr6:105529655..105531224hg19UCSC Ensembl
Innerchr6:105636348..105637917hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381570
hg191570
hg181570
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2418933, nssv2418936, nssv2418938, nssv2418935, nssv2418931, nssv2418930, nssv2418932, nssv2418934, nssv2418937, nssv2418939
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLIN28B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970156
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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