A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849644



Internal ID22624579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65339010..65340309hg38UCSC Ensembl
chr11:65106481..65107780hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458406
Samples
Known GenesDPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849644
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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