A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981555



Internal ID18270066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99749052..99758225hg38UCSC Ensembl
Innerchr7:99346675..99355848hg19UCSC Ensembl
Innerchr7:99184611..99193784hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg389174
hg199174
hg189174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2470915, nssv2470911, nssv2470909, nssv2470912, nssv2470910, nssv2470917, nssv2470916, nssv2470918, nssv2470913, nssv2470914
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCYP3A4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981555
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