A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285966



Internal ID20495184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195103308..195103308hg38UCSC Ensembl
chr3:194824037..194824037hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751660
Supporting Variants
Samples
Known GenesXXYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285966
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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