A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637314



Internal ID21829361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37099530..37099530hg38UCSC Ensembl
chr17:35456465..35456465hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091070
Supporting Variants
Samples
Known GenesACACA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637314
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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