A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977716



Internal ID18612922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51351082..51352504hg38UCSC Ensembl
Innerchr15:51643279..51644701hg19UCSC Ensembl
Innerchr15:49430571..49431993hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381423
hg191423
hg181423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2023444, nssv2023440, nssv2023441, nssv2023438, nssv2023445, nssv2023437, nssv2023439, nssv2023446, nssv2023442, nssv2023443
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGLDN
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977716
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