A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469774



Internal ID21127327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47008618..47010384hg38UCSC Ensembl
chr11:47030169..47031935hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381767
hg191767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991126
Samples
Known GenesC11orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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