A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581967



Internal ID20955038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98963280..98963973hg38UCSC Ensembl
chr12:99357058..99357751hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228300
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581967
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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