A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595704



Internal ID21787747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32412717..32412717hg38UCSC Ensembl
chr11:32434263..32434263hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081466
Supporting Variants
Samples
Known GenesWT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595704
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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