A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571819



Internal ID20944890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100418895..100419894hg38UCSC Ensembl
chr6:100866771..100867770hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270363
Samples
Known GenesSIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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