A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471759



Internal ID21129312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43601825..43602758hg38UCSC Ensembl
chr11:43623375..43624308hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38934
hg19934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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