A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454491



Internal ID21112044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8742873..8743369hg38UCSC Ensembl
chr11:8764420..8764916hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994944
Samples
Known GenesST5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454491
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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