A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739837



Internal ID20515813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29405057..29405123hg38UCSC Ensembl
chr4:29406679..29406745hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739837
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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