A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458906



Internal ID22516787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51451423..51453140hg38UCSC Ensembl
chr13:52025559..52027276hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381718
hg191718
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855081
Supporting Variants
Samples
Known GenesINTS6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458906
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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