A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397514



Internal ID22455384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33328340..33329070hg38UCSC Ensembl
chr19:33819246..33819976hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937514
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397514
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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