A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948134



Internal ID18594980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91464254..91479296hg38UCSC Ensembl
Innerchr10:93224011..93239053hg19UCSC Ensembl
Innerchr10:93213991..93229033hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3815043
hg1915043
hg1815043
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1862895, nssv1862892, nssv1862890, nssv1862897, nssv1862898, nssv1862899, nssv1862896, nssv1862893, nssv1862891, nssv1862894
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHECTD2, LOC100188947
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948134
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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