A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947738



Internal ID18594585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11624232..11629460hg38UCSC Ensembl
Innerchr10:11666231..11671459hg19UCSC Ensembl
Innerchr10:11706237..11711465hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385229
hg195229
hg185229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1831186, nssv1831187, nssv1831190, nssv1831183, nssv1831182, nssv1831181, nssv1831185, nssv1831184, nssv1831189, nssv1831188
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)nsv947738
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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