A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026565



Internal ID21935908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77913418..77921024hg38UCSC Ensembl
chr17:75909500..75917106hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg387607
hg197607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026565
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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