A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577611



Internal ID21769654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10489510..10517568hg38UCSC Ensembl
chr11:10511057..10539115hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3828059
hg1928059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036596
Supporting Variants
Samples
Known GenesAMPD3, MIR4485, MTRNR2L8, RNF141
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577611
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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