A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137679



Internal ID21501958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138537921..138538305hg38UCSC Ensembl
chr5:137873610..137873994hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582883
Supporting Variants
SamplesNA19239
Known GenesETF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137679
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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