A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523561



Internal ID20896922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8252088..8264851hg38UCSC Ensembl
chr19:8316972..8329735hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812764
hg1912764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049435
Samples
Known GenesCERS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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