A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980776



Internal ID18615976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181465154..181478259hg38UCSC Ensembl
Innerchr5:180892155..180905260hg19UCSC Ensembl
Innerchr5:180824761..180837969hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3813106
hg1913106
hg1813209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv69n82
Supporting Variantsnssv2392689, nssv2392694, nssv2392697, nssv2392690, nssv2392692, nssv2392693, nssv2392695, nssv2392691, nssv2392696, nssv2392698
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)nsv980776
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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