A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146083



Internal ID21407741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168283970..168284036hg38UCSC Ensembl
chr6:168684650..168684716hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582408
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146083
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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