A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271817



Internal ID20481035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2722504..2722744hg38UCSC Ensembl
chr2:2726276..2726516hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743174
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271817
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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