A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277452



Internal ID20486670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74117051..74117149hg38UCSC Ensembl
chr11:73828096..73828194hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730612
Supporting Variants
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277452
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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