A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984256



Internal ID18272758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8730034..8735592hg38UCSC Ensembl
Innerchr16:8823891..8829449hg19UCSC Ensembl
Innerchr16:8731392..8736950hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg385559
hg195559
hg185559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2041752, nssv2041753, nssv2041750, nssv2041747, nssv2041756, nssv2041749, nssv2041755, nssv2041748, nssv2041754, nssv2041751
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesABAT
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984256
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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