A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025184



Internal ID21934527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37296456..37296557hg38UCSC Ensembl
chr17:35653378..35653479hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629160
Samples
Known GenesACACA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025184
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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