A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081345



Internal ID21990578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1931942..1931942hg38UCSC Ensembl
chr17:1835236..1835236hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081345
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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