A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538437



Internal ID21862792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195167452..195167508hg38UCSC Ensembl
chr3:194888181..194888237hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992699
Supporting Variants
Samples
Known GenesXXYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538437
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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