A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515857



Internal ID20889218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32679724..32681616hg38UCSC Ensembl
chr19:33170630..33172522hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381893
hg191893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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