A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217554



Internal ID20784594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39129943..39130921hg38UCSC Ensembl
chr14:39599147..39600125hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38979
hg19979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579135
Supporting Variants
Samples
Known GenesGEMIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217554
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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