A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479300



Internal ID22537202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57476622..57492220hg38UCSC Ensembl
chr19:57987990..58003588hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3815599
hg1915599
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884545
Supporting Variants
Samples
Known GenesZNF419, ZNF772
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479300
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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