A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551231



Internal ID20924368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42601458..42605167hg38UCSC Ensembl
chr21:44021568..44025277hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383710
hg193710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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