A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528225



Internal ID20901586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54223458..54243259hg38UCSC Ensembl
chr19:54727330..54747108hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3819802
hg1919779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3719n223
Supporting Variantsnssv18048875
Samples
Known GenesLILRA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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