A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968959



Internal ID18604187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:84997203..85000693hg38UCSC Ensembl
Innerchr5:84293021..84296511hg19UCSC Ensembl
Innerchr5:84328777..84332267hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg383491
hg193491
hg183491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2367623, nssv2367628, nssv2367625, nssv2367619, nssv2367621, nssv2367622, nssv2367627, nssv2367620, nssv2367626, nssv2367624
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)nsv968959
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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