A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583081



Internal ID20956152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31976690..31977371hg38UCSC Ensembl
chr12:32129624..32130305hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236308
Samples
Known GenesKIAA1551
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583081
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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