A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947809



Internal ID18594656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:30511135..30518908hg38UCSC Ensembl
Innerchr10:30800064..30807837hg19UCSC Ensembl
Innerchr10:30840070..30847843hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg387774
hg197774
hg187774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1838412, nssv1838416, nssv1838419, nssv1838414, nssv1838418, nssv1838417, nssv1838420, nssv1838413, nssv1838421, nssv1838415
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)nsv947809
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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