A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419339



Internal ID22477209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133935961..133936581hg38UCSC Ensembl
chr5:133271652..133272272hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890605
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419339
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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