A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410193



Internal ID22468063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84532135..84532238hg38UCSC Ensembl
chr4:85453288..85453391hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410193
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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