A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266185



Internal ID20475403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209595423..209595848hg38UCSC Ensembl
chr2:210460147..210460572hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747226
Supporting Variants
Samples
Known GenesMAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266185
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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