A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130666



Internal ID21512300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1280101..1280150hg38UCSC Ensembl
chr4:1273889..1273938hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574105
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130666
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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