A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755393



Internal ID20531253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158245137..158245137hg38UCSC Ensembl
chr3:157962926..157962926hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288102
Samples
Known GenesRSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755393
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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