A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981103



Internal ID18616302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10116329..10123316hg38UCSC Ensembl
Innerchr6:10116562..10123549hg19UCSC Ensembl
Innerchr6:10224548..10231535hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg386988
hg196988
hg186988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2392898, nssv2392892, nssv2392900, nssv2392897, nssv2392899, nssv2392893, nssv2392901, nssv2392894, nssv2392895, nssv2392896
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)nsv981103
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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