A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981585



Internal ID18616782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134585315..134601314hg38UCSC Ensembl
Innerchr7:134270067..134286066hg19UCSC Ensembl
Innerchr7:133920607..133936606hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3816000
hg1916000
hg1816000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2478026, nssv2478025, nssv2478028, nssv2480650, nssv2480649, nssv2478027, nssv2480648, nssv2478029, nssv2480651, nssv2478030
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)nsv981585
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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