A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403171



Internal ID22461041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38876987..38877576hg38UCSC Ensembl
chr19:39367627..39368216hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927658
Supporting Variants
Samples
Known GenesRINL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403171
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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