A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141991



Internal ID21476768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3181831..3182010hg38UCSC Ensembl
chr6:3182065..3182244hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579338
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141991
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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