A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981568



Internal ID18616765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:105581565..105583038hg38UCSC Ensembl
Innerchr7:105222012..105223485hg19UCSC Ensembl
Innerchr7:105009248..105010721hg18UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg381474
hg191474
hg181474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2474918, nssv2474919, nssv2474920, nssv2474921, nssv2474922, nssv2474917, nssv2474924, nssv2474923, nssv2474926, nssv2474925
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)nsv981568
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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