A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516326



Internal ID20889687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44761518..44785226hg38UCSC Ensembl
chr19:45264775..45288483hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3823709
hg1923709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048193
Samples
Known GenesCBLC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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