A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525254



Internal ID20898615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38233002..38238381hg38UCSC Ensembl
chr19:38723642..38729021hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385380
hg195380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525254
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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