A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440971



Internal ID21098524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14726570..14727278hg38UCSC Ensembl
chr11:14748116..14748824hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988335
Samples
Known GenesPDE3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440971
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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