A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730528



Internal ID20506440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140009687..140014602hg38UCSC Ensembl
chr4:140930841..140935756hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg384916
hg194916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279962
Samples
Known GenesMAML3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730528
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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