A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966765



Internal ID18601995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26254413..26265220hg38UCSC Ensembl
Innerchr7:26294033..26304840hg19UCSC Ensembl
Innerchr7:26260558..26271365hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3810808
hg1910808
hg1810808
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2440625, nssv2440620, nssv2440624, nssv2440629, nssv2440626, nssv2440627, nssv2440623, nssv2440628, nssv2440621, nssv2440622
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)nsv966765
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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