A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732777



Internal ID20508702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10353319..10353382hg38UCSC Ensembl
chr11:10374866..10374929hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263476
Samples
Known GenesCAND1.11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732777
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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