A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733417



Internal ID20509347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6935568..6935627hg38UCSC Ensembl
chr2:7075699..7075758hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294918
Samples
Known GenesRNF144A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733417
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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