A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147472



Internal ID21508439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87010280..87010330hg38UCSC Ensembl
chr6:87719998..87720048hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567419
Supporting Variants
SamplesNA20509
Known GenesHTR1E
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147472
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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