A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439577



Internal ID21097130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13156066..13165615hg38UCSC Ensembl
chr11:13177613..13187162hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg389550
hg199550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987920
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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