A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930687



Internal ID22705958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34219872..34221500hg38UCSC Ensembl
chr19:34710777..34712405hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381629
hg191629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395754
Samples
Known GenesLSM14A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930687
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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