A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942642



Internal ID22718083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34272323..34272382hg38UCSC Ensembl
chr19:34763228..34763287hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400235
Samples
Known GenesKIAA0355
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942642
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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