A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752292



Internal ID20528152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55971634..55971634hg38UCSC Ensembl
chr1:56437307..56437307hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752292
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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