A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580604



Internal ID20953675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93611199..93625824hg38UCSC Ensembl
chr12:94004975..94019600hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3814626
hg1914626
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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