A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487407



Internal ID22545323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9516717..9518816hg38UCSC Ensembl
chr20:9497364..9499463hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885836
Supporting Variants
Samples
Known GenesLAMP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487407
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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