A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110643



Internal ID21293909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:8432546..8434846hg38UCSC Ensembl
Innerchr6:8432779..8435079hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1008n145
Supporting Variantsnssv14082987, nssv14082878, nssv14083596, nssv14083829, nssv14086488, nssv14083821, nssv14083047, nssv14083939
Samplessample154, sample413, sample41, sample347, sample387, sample302, sample331, sample386
Known GenesSLC35B3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110643
Frequency
Sample Size467
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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