A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294815



Internal ID20504033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162275440..162280763hg38UCSC Ensembl
chr5:161702446..161707769hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg385324
hg195324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747264
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294815
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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