A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412092



Internal ID22469962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61907877..61908030hg38UCSC Ensembl
chr5:61203704..61203857hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890784
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412092
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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