A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966989



Internal ID18602218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10064522..10066058hg38UCSC Ensembl
Innerchr3:10106206..10107742hg19UCSC Ensembl
Innerchr3:10081206..10082742hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381537
hg191537
hg181537
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2271656, nssv2271654, nssv2271653, nssv2271652, nssv2271657, nssv2271655, nssv2271658, nssv2271660, nssv2271661, nssv2271659
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFANCD2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966989
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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