A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737835



Internal ID20513799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105898304..105898361hg38UCSC Ensembl
chr4:106819461..106819518hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260459
Samples
Known GenesNPNT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737835
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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