A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584196



Internal ID20957267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10936082..10937170hg38UCSC Ensembl
chr10:10978045..10979133hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381089
hg191089
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228980
Samples
Known GenesLINC00710
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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