A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968878



Internal ID18257420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17060703..17067878hg38UCSC Ensembl
Innerchr5:17060812..17067987hg19UCSC Ensembl
Innerchr5:17113812..17120987hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg387176
hg197176
hg187176
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2347275, nssv2347273, nssv2347277, nssv2347271, nssv2347272, nssv2347268, nssv2347270, nssv2347274, nssv2347269, nssv2347276
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)nsv968878
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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