A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13702021



Internal ID21223845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58410520..58410757hg38UCSC Ensembl
chr19:58921887..58922124hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2799615
Supporting Variants
Samples
Known GenesZNF584
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13702021
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.55


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