A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570486



Internal ID20943557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168415646..168416797hg38UCSC Ensembl
chr6:168816326..168817477hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381152
hg191152
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570486
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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