A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591990



Internal ID20965061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56431817..56431994hg38UCSC Ensembl
chr12:56825601..56825778hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219845
Samples
Known GenesTIMELESS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591990
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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