A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575776



Internal ID20948847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41794883..41795909hg38UCSC Ensembl
chr15:42087081..42088107hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381027
hg191027
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238979
Samples
Known GenesMAPKBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575776
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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