A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517865



Internal ID20891226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5172799..5174019hg38UCSC Ensembl
chr19:5172810..5174030hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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