A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577152



Internal ID20950223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68576086..68576208hg38UCSC Ensembl
chr12:68969866..68969988hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577152
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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