A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138096



Internal ID21483108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144122533..144125412hg38UCSC Ensembl
chr4:145043686..145046565hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg382880
hg192880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583530
Supporting Variants
SamplesHG03732
Known GenesGYPA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138096
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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