A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585488



Internal ID20958559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45238597..45314447hg38UCSC Ensembl
chr17:43315964..43391813hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3875851
hg1975850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242361
Samples
Known GenesFMNL1, MAP3K14, MAP3K14-AS1, SPATA32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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