A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927773



Internal ID22703004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18655873..18662835hg38UCSC Ensembl
chr19:18766683..18773645hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg386963
hg196963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408626
Samples
Known GenesKLHL26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927773
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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