A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467062



Internal ID22524954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76552281..76559829hg38UCSC Ensembl
chr13:77126416..77133964hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg387549
hg197549
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467062
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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