A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241869



Internal ID20808909
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 StatusS
Merged Variantsnsv6586023
Supporting Variants
Samples
Known GenesGRAMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241869
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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