A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947841



Internal ID18594688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36725278..36744553hg38UCSC Ensembl
Innerchr10:37014206..37033481hg19UCSC Ensembl
Innerchr10:37054212..37073487hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3819276
hg1919276
hg1819276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1840799, nssv1840792, nssv1840795, nssv1840793, nssv1840797, nssv1840791, nssv1840796, nssv1840794, nssv1840798, nssv1840800
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)nsv947841
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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