A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529136



Internal ID21853493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27539692..27539786hg38UCSC Ensembl
chr2:27762559..27762653hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529136
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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