A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948215



Internal ID18595061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124488849..124493463hg38UCSC Ensembl
Innerchr10:126177418..126182032hg19UCSC Ensembl
Innerchr10:126167408..126172022hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384615
hg194615
hg184615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1870284, nssv1870283, nssv1870287, nssv1870290, nssv1870285, nssv1870286, nssv1870281, nssv1870288, nssv1870289, nssv1870282
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLHPP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948215
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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