A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856343



Internal ID22631278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96364903..96366302hg38UCSC Ensembl
chr14:96831240..96832639hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470395
Samples
Known GenesGSKIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856343
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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