A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578816



Internal ID20951887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51410608..51411321hg38UCSC Ensembl
chr12:51804392..51805105hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234785
Samples
Known GenesSLC4A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578816
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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