A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578819



Internal ID20951890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79876388..79880080hg38UCSC Ensembl
chr15:80168730..80172422hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383693
hg193693
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2601n223
Supporting Variantsnssv18239747
Samples
Known GenesMTHFS, ST20-MTHFS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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