A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097991



Internal ID22007224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27170237..27170237hg38UCSC Ensembl
chr17:25497263..25497263hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097991
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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