A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532694



Internal ID20906055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14140065..14144458hg38UCSC Ensembl
chr19:14250877..14255270hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg384394
hg194394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045907
Samples
Known GenesLOC100507373
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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