A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385923



Internal ID22443793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56882009..56890787hg38UCSC Ensembl
chr13:57456143..57464921hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg388779
hg198779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385923
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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