A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574099



Internal ID20947170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75370601..75372299hg38UCSC Ensembl
chr6:76080317..76082015hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381699
hg191699
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6268n223
Supporting Variantsnssv18272087
Samples
Known GenesFILIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574099
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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