A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530253



Internal ID20903614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38248791..38249234hg38UCSC Ensembl
chr19:38739431..38739874hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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