A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582398



Internal ID20955469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74211424..74212956hg38UCSC Ensembl
chr15:74503765..74505297hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381533
hg191533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582398
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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