A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039264



Internal ID21948607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:653635..653691hg38UCSC Ensembl
chr11:653635..653691hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596601
Samples
Known GenesDEAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039264
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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