A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981176



Internal ID18616375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113173200..113174480hg38UCSC Ensembl
Innerchr6:113494402..113495682hg19UCSC Ensembl
Innerchr6:113601095..113602375hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381281
hg191281
hg181281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2419393, nssv2419397, nssv2419399, nssv2419394, nssv2419391, nssv2419396, nssv2419392, nssv2419398, nssv2419395, nssv2419390
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)nsv981176
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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