A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555836



Internal ID20928907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152336791..152342231hg38UCSC Ensembl
chr3:152054580..152060020hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg385441
hg195441
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263232
Samples
Known GenesMBNL1, TMEM14E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555836
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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