A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080145



Internal ID21989378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3094543..3094543hg38UCSC Ensembl
chr4:3096270..3096270hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542894
Samples
Known GenesHTT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080145
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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