A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748187



Internal ID20524212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155800244..155800345hg38UCSC Ensembl
chr2:156656756..156656857hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748187
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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