A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573991



Internal ID20947062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160697667..160698720hg38UCSC Ensembl
chr6:161118699..161119752hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6470n223
Supporting Variantsnssv18270504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573991
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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