A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841712



Internal ID22616647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14324560..14325681hg38UCSC Ensembl
chr5:14324669..14325790hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495654
Samples
Known GenesTRIO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841712
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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