A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406611



Internal ID22464481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63619958..63624717hg38UCSC Ensembl
chr20:62251311..62256070hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384760
hg194760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957357
Supporting Variants
Samples
Known GenesGMEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406611
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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