A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153584



Internal ID21488148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53305353..53305402hg38UCSC Ensembl
chr6:53170151..53170200hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569061
Supporting Variants
SamplesNA18534
Known GenesELOVL5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153584
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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