A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036189



Internal ID21945532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32657100..32668151hg38UCSC Ensembl
chr11:32678646..32689697hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3811052
hg1911052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580086
Samples
Known GenesCCDC73
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036189
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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