A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038833



Internal ID21948176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83139458..83173878hg38UCSC Ensembl
chr17:81087227..81121647hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3834421
hg1934421
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636667
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038833
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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