A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571694



Internal ID20944765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139444396..139445939hg38UCSC Ensembl
chr6:139765533..139767076hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381544
hg191544
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571694
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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