A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981144



Internal ID18616343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52827109..52882917hg38UCSC Ensembl
Innerchr6:52691907..52747715hg19UCSC Ensembl
Innerchr6:52799866..52855674hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3855809
hg1955809
hg1855809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2409335, nssv2409334, nssv2409332, nssv2409329, nssv2409327, nssv2409330, nssv2409333, nssv2409328, nssv2409331, nssv2409326
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGSTA5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981144
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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