A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533558



Internal ID21857914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27288976..27289029hg38UCSC Ensembl
chr1:27615467..27615520hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5983644
Supporting Variants
Samples
Known GenesWDTC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533558
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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