A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260459



Internal ID20469677
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 StatusS
Merged Variantsnsv4737835
Supporting Variants
Samples
Known GenesNPNT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260459
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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