A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964913



Internal ID18600149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99521566..99531565hg38UCSC Ensembl
Innerchr5:98857270..98867269hg19UCSC Ensembl
Innerchr5:98885169..98895168hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3810000
hg1910000
hg1810000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2701642, nssv2701636, nssv2701584, nssv2701582, nssv2701581, nssv2701576, nssv2701634, nssv2701575, nssv2701580, nssv2701579, nssv2701643, nssv2701577, nssv2701635, nssv2701641, nssv2701578, nssv2701583, nssv2701640, nssv2701639, nssv2701638, nssv2701637
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964913
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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