A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500371



Internal ID22558308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85285820..85295425hg38UCSC Ensembl
chr5:84581638..84591243hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg389606
hg199606
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500371
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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