A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585260



Internal ID20958331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92902741..92902937hg38UCSC Ensembl
chr12:93296517..93296713hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227784
Samples
Known GenesEEA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585260
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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