A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15184695



Internal ID21323491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:17143786..17143900hg38UCSC Ensembl
chr16:17237643..17237757hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3932046
Supporting Variants
SamplesHG002
Known GenesXYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15184695
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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