A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463706



Internal ID21121259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73203051..73203990hg38UCSC Ensembl
chr11:72914096..72915035hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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