A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741736



Internal ID20517714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100037396..100037547hg38UCSC Ensembl
chr2:100653858..100654009hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291521
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741736
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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