A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436969



Internal ID21094522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8027584..8029458hg38UCSC Ensembl
chr11:8049131..8051005hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381875
hg191875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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