A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487332



Internal ID22545248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63619833..63624732hg38UCSC Ensembl
chr20:62251186..62256085hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877847
Supporting Variants
Samples
Known GenesGMEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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