A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130058



Internal ID21480868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175355615..175356316hg38UCSC Ensembl
chr5:174782618..174783319hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577872
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130058
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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