A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579961



Internal ID20953032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37376619..37416337hg38UCSC Ensembl
chr14:37845824..37885542hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3839719
hg1939719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231142
Samples
Known GenesMIPOL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579961
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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