A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948106



Internal ID18594952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84081449..84085840hg38UCSC Ensembl
Innerchr10:85841205..85845596hg19UCSC Ensembl
Innerchr10:85831185..85835576hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384392
hg194392
hg184392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1859037, nssv1859042, nssv1859041, nssv1859044, nssv1859038, nssv1859039, nssv1859040, nssv1859036, nssv1859043, nssv1859035
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)nsv948106
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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