A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076476



Internal ID21985709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3094675..3094675hg38UCSC Ensembl
chr4:3096402..3096402hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544481
Samples
Known GenesHTT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076476
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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