A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740632



Internal ID20516608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173957332..173957650hg38UCSC Ensembl
chr4:174878483..174878801hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740632
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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