A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472354



Internal ID21129907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34293059..34303673hg38UCSC Ensembl
chr11:34314606..34325220hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3810615
hg1910615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990842
Samples
Known GenesABTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472354
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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