A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974821



Internal ID18610030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:61053419..61056424hg38UCSC Ensembl
Innerchr16:61087323..61090328hg19UCSC Ensembl
Innerchr16:59644824..59647829hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383006
hg193006
hg183006
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2063651, nssv2063652, nssv2063654, nssv2063647, nssv2063648, nssv2063653, nssv2063655, nssv2063649, nssv2063650, nssv2063646
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)nsv974821
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