A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112191



Internal ID21295457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71952688..72044054hg38UCSC Ensembl
Innerchr3:72001839..72093205hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3891367
hg1991367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108135
Samplessample203
Known GenesLINC00877
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112191
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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