A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466176



Internal ID21123729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47252827..47253089hg38UCSC Ensembl
chr11:47274378..47274640hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991140
Samples
Known GenesNR1H3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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