A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589537



Internal ID20962608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101602240..101603266hg38UCSC Ensembl
chr12:101996018..101997044hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg381027
hg191027
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219066
Samples
Known GenesMYBPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589537
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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