A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977706



Internal ID18266226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44560392..44562094hg38UCSC Ensembl
Innerchr15:44852590..44854292hg19UCSC Ensembl
Innerchr15:42639882..42641584hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg381703
hg191703
hg181703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2021609, nssv2021603, nssv2021610, nssv2021608, nssv2021611, nssv2021604, nssv2021607, nssv2021602, nssv2021605, nssv2021606
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesEIF3J
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977706
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