A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020988



Internal ID21930331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47255586..47255665hg38UCSC Ensembl
chr11:47277137..47277216hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588495
Samples
Known GenesNR1H3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020988
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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