A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947855



Internal ID18594702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38079145..38081969hg38UCSC Ensembl
Innerchr10:38368073..38370897hg19UCSC Ensembl
Innerchr10:38408079..38410903hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg382825
hg192825
hg182825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1841218, nssv1841214, nssv1841219, nssv1841213, nssv1841215, nssv1841212, nssv1841217, nssv1841220, nssv1841216, nssv1841221
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)nsv947855
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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