A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071996



Internal ID21981229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165357923..165357923hg38UCSC Ensembl
chr4:166279075..166279075hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071996
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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