A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588729



Internal ID20961800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95008406..95008657hg38UCSC Ensembl
chr12:95402182..95402433hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588729
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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