A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525292



Internal ID20898653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8345601..8349600hg38UCSC Ensembl
chr19:8410485..8414484hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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