A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440351



Internal ID21097904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:413274..452482hg38UCSC Ensembl
chr11:413274..452482hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3839209
hg1939209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991404
Samples
Known GenesANO9, PTDSS2, SIGIRR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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