A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465599



Internal ID22523488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112108204..112112365hg38UCSC Ensembl
chr13:112762518..112766679hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg384162
hg194162
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465599
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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