A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555507



Internal ID20928593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33806038..33808014hg38UCSC Ensembl
chr21:35178342..35180318hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381977
hg191977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203918
Samples
Known GenesITSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555507
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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