A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523905



Internal ID20897266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45399386..45415052hg38UCSC Ensembl
chr19:45902644..45918310hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3815667
hg1915667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048660
Samples
Known GenesCD3EAP, ERCC1, PPP1R13L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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