A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586023



Internal ID20959094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72171325..72175178hg38UCSC Ensembl
chr15:72463666..72467519hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383854
hg193854
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241869
Samples
Known GenesGRAMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586023
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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