A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394321



Internal ID22452191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13810258..13810551hg38UCSC Ensembl
chr19:13921072..13921365hg19UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944163
Supporting Variants
Samples
Known GenesZSWIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394321
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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