A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970452



Internal ID18605674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24906090..24906975hg38UCSC Ensembl
Innerchr7:24945709..24946594hg19UCSC Ensembl
Innerchr7:24912234..24913119hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38886
hg19886
hg18886
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2439942, nssv2439940, nssv2439944, nssv2439943, nssv2439937, nssv2439941, nssv2439938, nssv2439939, nssv2439945, nssv2439936
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOSBPL3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970452
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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