A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158351



Internal ID21479998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6185335..6185422hg38UCSC Ensembl
chr6:6185568..6185655hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570905
Supporting Variants
SamplesHG03683
Known GenesF13A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158351
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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