A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066342



Internal ID21410291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8087242..8087593hg38UCSC Ensembl
chr1:8147302..8147653hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582186
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066342
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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