A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931491



Internal ID22706776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18591378..18591690hg38UCSC Ensembl
chr19:18702188..18702500hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395532
Samples
Known GenesC19orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931491
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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