A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585007



Internal ID20958078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31419448..31420390hg38UCSC Ensembl
chr12:31572382..31573324hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38943
hg19943
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222023
Samples
Known GenesDENND5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585007
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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