A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17554461



Internal ID21878816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27513420..27513516hg38UCSC Ensembl
chr3:27554911..27555007hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17554461
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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