A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981465



Internal ID18616662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45825162..45859806hg38UCSC Ensembl
Innerchr7:45864761..45899405hg19UCSC Ensembl
Innerchr7:45831286..45865930hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3834645
hg1934645
hg1834645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2446311, nssv2446307, nssv2446312, nssv2446305, nssv2446308, nssv2446313, nssv2446310, nssv2446306, nssv2446304, nssv2446309
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)nsv981465
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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