A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524192



Internal ID20897553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24590039..24590319hg38UCSC Ensembl
chr20:24570675..24570955hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068765
Samples
Known GenesSYNDIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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