A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064667



Internal ID21973900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82695012..82695012hg38UCSC Ensembl
chr4:83616165..83616165hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537698
Samples
Known GenesSCD5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064667
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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