A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933809



Internal ID22709126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42436057..42436202hg38UCSC Ensembl
chr19:42940209..42940354hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401940
Samples
Known GenesCXCL17, LIPE-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933809
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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