A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125184



Internal ID21463907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140302934..140302987hg38UCSC Ensembl
chr4:141224088..141224141hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577928
Supporting Variants
SamplesHG03065
Known GenesLOC100129858, SCOC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125184
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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