A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547507



Internal ID20920708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54030531..54041463hg38UCSC Ensembl
chr20:52647070..52658002hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3810933
hg1910933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4494n223
Supporting Variantsnssv18067901
Samples
Known GenesBCAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547507
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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