A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123766



Internal ID21462658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154475275..154538487hg38UCSC Ensembl
chr4:155396427..155459639hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3863213
hg1963213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574634
Supporting Variants
SamplesHG03009
Known GenesDCHS2, PLRG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123766
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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