A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555235



Internal ID21879590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3143283..3143374hg38UCSC Ensembl
chr4:3145010..3145101hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996913
Supporting Variants
Samples
Known GenesHTT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555235
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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