A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974840



Internal ID18610049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87268171..87269474hg38UCSC Ensembl
Innerchr16:87301777..87303080hg19UCSC Ensembl
Innerchr16:85859278..85860581hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381304
hg191304
hg181304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2070566, nssv2070562, nssv2070568, nssv2070569, nssv2070565, nssv2070567, nssv2070564, nssv2070570, nssv2070561, nssv2070563
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)nsv974840
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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