A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895181



Internal ID22670259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117046748..117052252hg38UCSC Ensembl
chr5:116382444..116387948hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg385505
hg195505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1708n209
Supporting Variantsnssv17424258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895181
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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