A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037411



Internal ID21946754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3925663..3949739hg38UCSC Ensembl
chr11:3946893..3970969hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824077
hg1924077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593544
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037411
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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