A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847929



Internal ID22622864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81383449..81384498hg38UCSC Ensembl
chr14:81849793..81850842hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461989
Samples
Known GenesSTON2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847929
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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