A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485936



Internal ID22543849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38034579..38037303hg38UCSC Ensembl
chr20:36662981..36665705hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg382725
hg192725
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870206
Supporting Variants
Samples
Known GenesRPRD1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485936
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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