A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532861



Internal ID20906222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44083401..44092700hg38UCSC Ensembl
chr19:44587554..44596853hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048143
Samples
Known GenesZNF284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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