A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470570



Internal ID21128123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86593201..86596700hg38UCSC Ensembl
chr11:86304243..86307742hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994627
Samples
Known GenesME3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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