A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094546



Internal ID21467479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52624054..52626744hg38UCSC Ensembl
chr13:53198189..53200879hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg382691
hg192691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589522
Supporting Variants
SamplesHG03065
Known GenesHNRNPA1L2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094546
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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