A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467517



Internal ID21125070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103939601..103941000hg38UCSC Ensembl
chr11:103810329..103811728hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986044
Samples
Known GenesPDGFD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467517
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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