A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538038



Internal ID20911364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44571001..44737900hg38UCSC Ensembl
chr21:45990884..46157815hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38166900
hg19166932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073308
Samples
Known GenesKRTAP10-10, KRTAP10-11, KRTAP10-12, KRTAP10-4, KRTAP10-5, KRTAP10-6, KRTAP10-7, KRTAP10-8, KRTAP10-9, KRTAP12-1, KRTAP12-2, KRTAP12-3, KRTAP12-4, TSPEAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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