A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520516



Internal ID20893877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55138089..55164347hg38UCSC Ensembl
chr19:55649457..55675715hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3826259
hg1926259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049144
Samples
Known GenesDNAAF3, TNNI3, TNNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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