A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384764



Internal ID22442634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57302775..57477218hg38UCSC Ensembl
chr13:57876909..58051352hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38174444
hg19174444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930377
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384764
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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