A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765569



Internal ID20541429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68975338..68975338hg38UCSC Ensembl
chr17:66971479..66971479hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275603
Samples
Known GenesABCA9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765569
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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