A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158001



Internal ID21494079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170191552..170191817hg38UCSC Ensembl
chr6:170506776..170507041hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567781
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158001
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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