A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410442



Internal ID22468312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40262961..40264640hg38UCSC Ensembl
chr5:40263063..40264742hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg381680
hg191680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410442
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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