A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577806



Internal ID20950877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121874437..121874936hg38UCSC Ensembl
chr12:122312343..122312842hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229543
Samples
Known GenesHPD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577806
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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