A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130759



Internal ID21440538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153724962..153725042hg38UCSC Ensembl
chr4:154646114..154646194hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583659
Supporting Variants
SamplesHG00732
Known GenesRNF175
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130759
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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