A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532903



Internal ID20906264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55397301..55399200hg38UCSC Ensembl
chr19:55908669..55910568hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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