A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970617



Internal ID18605839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152820860..152847348hg38UCSC Ensembl
Innerchr7:152517945..152544433hg19UCSC Ensembl
Innerchr7:152148878..152175366hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3826489
hg1926489
hg1826489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2489183, nssv2489175, nssv2489178, nssv2489181, nssv2489179, nssv2489182, nssv2489184, nssv2489176, nssv2489180, nssv2489177
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesACTR3B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970617
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