A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128025



Internal ID21480177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144123456..144124050hg38UCSC Ensembl
chr4:145044609..145045203hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573766
Supporting Variants
SamplesHG03683
Known GenesGYPA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128025
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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