A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948174



Internal ID18595020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103215015..103230012hg38UCSC Ensembl
Innerchr10:104974772..104989769hg19UCSC Ensembl
Innerchr10:104964762..104979759hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3814998
hg1914998
hg1814998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1865212, nssv1865213, nssv1865204, nssv1865207, nssv1865206, nssv1865205, nssv1865209, nssv1865210, nssv1865211, nssv1865208
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)nsv948174
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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