A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523703



Internal ID20897064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39995691..39997770hg38UCSC Ensembl
chr19:40501598..40503677hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382080
hg192080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047915
Samples
Known GenesZNF546
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523703
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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