A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565700



Internal ID20938771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6173441..6174166hg38UCSC Ensembl
chr6:6173674..6174399hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271616
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565700
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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