A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120437



Internal ID21506971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195150870..195150870hg38UCSC Ensembl
chr3:194871599..194871599hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609562
Supporting Variants
SamplesNA19983
Known GenesXXYLT1, XXYLT1-AS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120437
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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