A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473565



Internal ID21131118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95076962..95094929hg38UCSC Ensembl
chr11:94810126..94828093hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3817968
hg1917968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995543
Samples
Known GenesENDOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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