A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546352



Internal ID20919570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44332501..44603700hg38UCSC Ensembl
chr21:45752384..46023617hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38271200
hg19271234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073285
Samples
Known GenesC21orf2, C21orf90, KRTAP10-1, KRTAP10-2, KRTAP10-3, KRTAP10-4, KRTAP10-5, KRTAP10-6, KRTAP10-7, LRRC3, LRRC3-AS1, TRPM2, TSPEAR, TSPEAR-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546352
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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