A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451761



Internal ID22509633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76560073..76602559hg38UCSC Ensembl
chr13:77134208..77176694hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3842487
hg1942487
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857250
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451761
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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