A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271861



Internal ID20481079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1940885..1940942hg38UCSC Ensembl
chr4:1942612..1942669hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743161
Supporting Variants
Samples
Known GenesWHSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271861
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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