A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532755



Internal ID20906116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3899141..3901153hg38UCSC Ensembl
chr19:3899139..3901151hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382013
hg192013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047837
Samples
Known GenesATCAY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532755
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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