A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457449



Internal ID22515331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85688337..85696313hg38UCSC Ensembl
chr13:86262472..86270448hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg387977
hg197977
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457449
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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