A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947821



Internal ID18594668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32186384..32189908hg38UCSC Ensembl
Innerchr10:32475312..32478836hg19UCSC Ensembl
Innerchr10:32515318..32518842hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383525
hg193525
hg183525
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1838040, nssv1838046, nssv1838038, nssv1838045, nssv1838043, nssv1838037, nssv1838044, nssv1838042, nssv1838041, nssv1838039
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)nsv947821
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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