A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395532



Internal ID22453402
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 StatusS
Merged Variantsnsv5931491
Supporting Variants
Samples
Known GenesC19orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395532
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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