A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486096



Internal ID22544009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49090005..49118647hg38UCSC Ensembl
chr20:47706542..47735184hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3828643
hg1928643
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885318
Supporting Variants
Samples
Known GenesCSE1L, STAU1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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