A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532611



Internal ID20905972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58371197..58377173hg38UCSC Ensembl
chr19:58882564..58888540hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385977
hg195977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049903
Samples
Known GenesZNF837
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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