A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376292



Internal ID22601961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76007689..76008465hg38UCSC Ensembl
chr13:76581825..76582601hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38777
hg19777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938482
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376292
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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