A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557218



Internal ID20930289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39122206..39123386hg38UCSC Ensembl
chr8:38979725..38980905hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277952
Samples
Known GenesADAM32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557218
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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