A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465763



Internal ID22523652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19838807..19840106hg38UCSC Ensembl
chr13:20412947..20414246hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858415
Supporting Variants
Samples
Known GenesZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465763
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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