A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574042



Internal ID20947113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85567721..85569191hg38UCSC Ensembl
chr6:86277439..86278909hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg381471
hg191471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274825
Samples
Known GenesSNX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574042
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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