A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399305



Internal ID22457175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39387653..39412021hg38UCSC Ensembl
chr19:39878293..39902661hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3824369
hg1924369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944000
Supporting Variants
Samples
Known GenesMED29, MIR4530, PAF1, ZFP36
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399305
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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