A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972419



Internal ID18607635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92676645..92678148hg38UCSC Ensembl
Innerchr9:95438927..95440430hg19UCSC Ensembl
Innerchr9:94478748..94480251hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381504
hg191504
hg181504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2557944, nssv2557946, nssv2557949, nssv2557951, nssv2557945, nssv2557943, nssv2557948, nssv2557947, nssv2557950, nssv2557952
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)nsv972419
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