A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068967



Internal ID21978200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94658889..94658889hg38UCSC Ensembl
chr5:93994594..93994594hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543016
Samples
Known GenesANKRD32
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068967
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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