A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499304



Internal ID22557239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102773963..102779645hg38UCSC Ensembl
chr5:102109667..102115349hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg385683
hg195683
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499304
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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