A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457395



Internal ID21114948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44091963..44093759hg38UCSC Ensembl
chr11:44113513..44115309hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381797
hg191797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457395
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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