A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461061



Internal ID22518944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35571983..35579273hg38UCSC Ensembl
chr13:36146120..36153410hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg387291
hg197291
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859555
Supporting Variants
Samples
Known GenesMIR548F5, NBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461061
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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