A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557794



Internal ID20930865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38123920..38125582hg38UCSC Ensembl
chr8:37981438..37983100hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg381663
hg191663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277901
Samples
Known GenesASH2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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