A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964971



Internal ID18600206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:174914012..174931792hg38UCSC Ensembl
Innerchr5:174341015..174358795hg19UCSC Ensembl
Innerchr5:174273621..174291401hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3817781
hg1917781
hg1817781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2386580, nssv2386578, nssv2386575, nssv2386576, nssv2386582, nssv2386573, nssv2386581, nssv2386579, nssv2386574, nssv2386577
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFLJ16171
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964971
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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