A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576192



Internal ID20949263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15811960..15816198hg38UCSC Ensembl
chr10:15853959..15858197hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384239
hg194239
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv618n223
Supporting Variantsnssv18233190
Samples
Known GenesFAM188A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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