A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560150



Internal ID20933221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79987439..79988241hg38UCSC Ensembl
chr5:79283262..79284064hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270323
Samples
Known GenesMTX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560150
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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