A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477964



Internal ID22535865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52303222..52317516hg38UCSC Ensembl
chr19:52806475..52820769hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3814295
hg1914295
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878298
Supporting Variants
Samples
Known GenesZNF480
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477964
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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