A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982454



Internal ID18617649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62370737..62387645hg38UCSC Ensembl
Innerchr9:46682038..46698946hg19UCSC Ensembl
Innerchr9:46522034..46538942hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3816909
hg1916909
hg1816909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2737605, nssv2737602, nssv2737599, nssv2737608, nssv2737607, nssv2737601, nssv2737600, nssv2737604, nssv2737603, nssv2737606
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKGFLP1, LOC643648
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982454
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