A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451844



Internal ID22509716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88012729..88036431hg38UCSC Ensembl
chr13:88664984..88688686hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3823703
hg1923703
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451844
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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