A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550525



Internal ID20923666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18364192..18364742hg38UCSC Ensembl
chr21:19736509..19737059hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069510
Samples
Known GenesTMPRSS15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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