A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472747



Internal ID21130300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107548703..107555635hg38UCSC Ensembl
chr11:107419429..107426361hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg386933
hg196933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986554
Samples
Known GenesALKBH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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