A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094572



Internal ID22003805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68898116..68898116hg38UCSC Ensembl
chr17:66894257..66894257hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619899
Samples
Known GenesABCA8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094572
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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