A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532737



Internal ID20906098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15608589..15612021hg38UCSC Ensembl
chr19:15719400..15722832hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383433
hg193433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532737
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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