A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943102



Internal ID22718546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34919547..36186973hg38UCSC Ensembl
chr16:34173151..35285801hg19UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg381267427
hg191112651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376782
Samples
Known GenesFLJ26245, LOC100130700, LOC146481, LOC283914, UBE2MP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943102
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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