A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468810



Internal ID21126363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36625901..36630200hg38UCSC Ensembl
chr11:36647451..36651750hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989928
Samples
Known GenesC11orf74
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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