A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948131



Internal ID18594977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89139752..89140449hg38UCSC Ensembl
Innerchr10:90899509..90900206hg19UCSC Ensembl
Innerchr10:90889489..90890186hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38698
hg19698
hg18698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1862340, nssv1862341, nssv1862343, nssv1862344, nssv1862345, nssv1862338, nssv1862339, nssv1862342, nssv1862347, nssv1862346
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)nsv948131
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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