A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966767



Internal ID18601997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26980197..26983748hg38UCSC Ensembl
Innerchr7:27019816..27023367hg19UCSC Ensembl
Innerchr7:26986341..26989892hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg383552
hg193552
hg183552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2439514, nssv2439512, nssv2439510, nssv2439506, nssv2439513, nssv2439515, nssv2439509, nssv2439511, nssv2439508, nssv2439507
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966767
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