A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552381



Internal ID20925508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40492313..40492755hg38UCSC Ensembl
chr21:41864240..41864682hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072737
Samples
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552381
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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