A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461168



Internal ID22519051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49900244..49905539hg38UCSC Ensembl
chr13:50474380..50479675hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg385296
hg195296
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860663
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461168
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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