A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111236



Internal ID21294502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9164276..9179255hg38UCSC Ensembl
Innerchr19:9274952..9289931hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3814980
hg1914980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv548n145
Supporting Variantsnssv14099624, nssv14101545, nssv14101509, nssv14101572, nssv14100496, nssv14101478, nssv14101215, nssv14101049, nssv14101257, nssv14101164, nssv14101218, nssv14100516, nssv14101353, nssv14101371, nssv14101032, nssv14101521, nssv14101445, nssv14102866, nssv14101147, nssv14100405, nssv14101116, nssv14101377, nssv14101455
Samplessample346, sample78, sample171, sample369, sample52, sample358, sample95, sample58, sample211, sample310, sample383, sample19, sample44, sample387, sample375, sample217, sample343, sample118, sample79, sample302, sample364, sample309, sample27
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111236
Frequency
Sample Size467
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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