A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937626



Internal ID22712997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33056944..33062605hg38UCSC Ensembl
chr19:33547850..33553511hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg385662
hg195662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398538
Samples
Known GenesRHPN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937626
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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