A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032437



Internal ID21941780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:26937336..26940879hg38UCSC Ensembl
chr17:25264362..25267905hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg383544
hg193544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032437
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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