A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970172



Internal ID18258710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149914112..149923319hg38UCSC Ensembl
Innerchr6:150235248..150244455hg19UCSC Ensembl
Innerchr6:150276941..150286148hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg389208
hg199208
hg189208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2427261, nssv2427256, nssv2427258, nssv2427262, nssv2427255, nssv2427263, nssv2427254, nssv2427259, nssv2427257, nssv2427260
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRAET1E-AS1, RAET1G
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970172
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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