A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474637



Internal ID22532531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29036274..29040914hg38UCSC Ensembl
chr19:29527181..29531821hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg384641
hg194641
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880718
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474637
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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