A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966757



Internal ID18601987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6805121..6809440hg38UCSC Ensembl
Innerchr7:6844752..6849071hg19UCSC Ensembl
Innerchr7:6811277..6815596hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg384320
hg194320
hg184320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2435321, nssv2435322, nssv2435325, nssv2435324, nssv2435327, nssv2435326, nssv2435328, nssv2435323, nssv2435329, nssv2435320
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCZ1B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966757
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