A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146571



Internal ID345776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17773327..17776321hg38UCSC Ensembl
chr21:19145644..19148638hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg382995
hg192995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146571
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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