A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025051



Internal ID21934394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78301695..78304492hg38UCSC Ensembl
chr11:78012741..78015538hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382798
hg192798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595418
Samples
Known GenesGAB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025051
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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