A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580037



Internal ID20953108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:87998702..88000545hg38UCSC Ensembl
chr12:88392479..88394322hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg381844
hg191844
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1646n223
Supporting Variantsnssv18225990
Samples
Known GenesC12orf50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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