A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469256



Internal ID21126809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72121375..72124052hg38UCSC Ensembl
chr11:71832421..71835098hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382678
hg192678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992768
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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