A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528980



Internal ID20902341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44736936..44741987hg38UCSC Ensembl
chr19:45240193..45245244hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg385052
hg195052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528980
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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