A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970171



Internal ID18605395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149593935..149594527hg38UCSC Ensembl
Innerchr6:149915071..149915663hg19UCSC Ensembl
Innerchr6:149956764..149957356hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38593
hg19593
hg18593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2426635, nssv2426634, nssv2426633, nssv2426636, nssv2426630, nssv2426637, nssv2426638, nssv2426632, nssv2426631, nssv2426629
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRPS18P9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970171
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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