A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970141



Internal ID18605365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71165715..71169074hg38UCSC Ensembl
Innerchr6:71875418..71878777hg19UCSC Ensembl
Innerchr6:71932139..71935498hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg383360
hg193360
hg183360
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2413819, nssv2413816, nssv2413821, nssv2413822, nssv2413818, nssv2413820, nssv2413813, nssv2413815, nssv2413814, nssv2413817
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970141
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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