A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420561



Internal ID22478431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66522267..66522568hg38UCSC Ensembl
chr5:65818095..65818396hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901271
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420561
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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