A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524855



Internal ID20898216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2273307..2274758hg38UCSC Ensembl
chr19:2273306..2274757hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381452
hg191452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045244
Samples
Known GenesC19orf35, OAZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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