A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535810



Internal ID20909163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44473788..44670842hg38UCSC Ensembl
chr21:45893671..46090759hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38197055
hg19197089
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204138
Samples
Known GenesC21orf90, KRTAP10-1, KRTAP10-10, KRTAP10-11, KRTAP10-2, KRTAP10-3, KRTAP10-4, KRTAP10-5, KRTAP10-6, KRTAP10-7, KRTAP10-8, KRTAP10-9, KRTAP12-2, KRTAP12-3, KRTAP12-4, TSPEAR, TSPEAR-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535810
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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