A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524674



Internal ID20898035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35627586..35628057hg38UCSC Ensembl
chr19:36118488..36118959hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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