A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977936



Internal ID18613141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21730229..21754816hg38UCSC Ensembl
Innerchr16:21741550..21766137hg19UCSC Ensembl
Innerchr16:21649051..21673638hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3824588
hg1924588
hg1824588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2052616, nssv2052612, nssv2052618, nssv2052614, nssv2052620, nssv2052619, nssv2052621, nssv2052615, nssv2052613, nssv2052617
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOTOA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977936
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer