A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734519



Internal ID20510456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:108462210..108462270hg38UCSC Ensembl
chr2:109078666..109078726hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269482
Samples
Known GenesGCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734519
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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