A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112818



Internal ID21296084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82739305..82740459hg38UCSC Ensembl
Innerchr14:83205649..83206803hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095225, nssv14096256, nssv14095364, nssv14095236, nssv14095142, nssv14095062, nssv14094116, nssv14094074, nssv14095246, nssv14094191, nssv14095162, nssv14095460, nssv14093960, nssv14095423, nssv14095187, nssv14096253, nssv14095598, nssv14094108, nssv14093973, nssv14093956, nssv14095182, nssv14095577, nssv14095488, nssv14094143
Samplessample60, sample50, sample225, sample142, sample369, sample285, sample383, sample416, sample387, sample32, sample407, sample378, sample290, sample79, sample175, sample245, sample187, sample331, sample234, sample286, sample46, sample246, sample163, sample411
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112818
Frequency
Sample Size467
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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