A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561702



Internal ID20934773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38390351..38390933hg38UCSC Ensembl
chr8:38247869..38248451hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277930
Samples
Known GenesLETM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561702
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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