A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587294



Internal ID20960365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80826638..80827196hg38UCSC Ensembl
chr12:81220417..81220975hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233778
Samples
Known GenesLIN7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587294
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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