A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537810



Internal ID20911142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44799147..44799868hg38UCSC Ensembl
chr21:46219062..46219783hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073334
Samples
Known GenesUBE2G2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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