A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577982



Internal ID20951053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1693111..1693819hg38UCSC Ensembl
chr12:1802277..1802985hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221429
Samples
Known GenesADIPOR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577982
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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