A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468677



Internal ID22526566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97705276..97708105hg38UCSC Ensembl
chr13:98357530..98360359hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg382830
hg192830
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855821
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468677
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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