A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464311



Internal ID22522197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56157238..56160037hg38UCSC Ensembl
chr13:56731372..56734171hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860469
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464311
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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