A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964815



Internal ID18600051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1608816..1639202hg38UCSC Ensembl
Innerchr5:1608931..1639317hg19UCSC Ensembl
Innerchr5:1661931..1692317hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3830387
hg1930387
hg1830387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2346097, nssv2346091, nssv2346098, nssv2346095, nssv2346089, nssv2346094, nssv2346096, nssv2346093, nssv2346090, nssv2346092
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC728613
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964815
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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