A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524575



Internal ID20897936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2330782..2343494hg38UCSC Ensembl
chr19:2330781..2343492hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812713
hg1912712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045300
Samples
Known GenesSPPL2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524575
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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