A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479332



Internal ID22537234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58240294..58244111hg38UCSC Ensembl
chr19:58751660..58755477hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383818
hg193818
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868403
Supporting Variants
Samples
Known GenesZNF544
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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