A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522587



Internal ID20895948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29772896..29773884hg38UCSC Ensembl
chr19:30263803..30264791hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38989
hg19989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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