A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583285



Internal ID20956356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31988964..31989177hg38UCSC Ensembl
chr12:32141898..32142111hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222093
Samples
Known GenesKIAA1551
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583285
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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