A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562619



Internal ID20935690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14695339..14696903hg38UCSC Ensembl
chr6:14695570..14697134hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562619
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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