A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127971



Internal ID21478401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42813983..42814095hg38UCSC Ensembl
chr5:42814085..42814197hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567825
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127971
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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