A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382683



Internal ID22440553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98627018..98633923hg38UCSC Ensembl
chr13:99279272..99286177hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg386906
hg196906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935307
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382683
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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