A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588129



Internal ID20961200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31403677..31404861hg38UCSC Ensembl
chr12:31556611..31557795hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229888
Samples
Known GenesDENND5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588129
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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