A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747226



Internal ID20523243
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 StatusM
Merged Variants
Supporting Variantsnssv16266185
Samples
Known GenesMAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747226
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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