A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583557



Internal ID20956628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83827655..83865636hg38UCSC Ensembl
chr15:84496407..84534388hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3837982
hg1937982
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240451
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583557
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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