A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563189



Internal ID21887544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161998583..162002990hg38UCSC Ensembl
chr5:161425589..161429996hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg384408
hg194408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563189
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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