A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091814



Internal ID22001047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94609581..94609581hg38UCSC Ensembl
chr11:94342747..94342747hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593340
Samples
Known GenesPIWIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091814
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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