A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240429



Internal ID20807469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83025047..83026078hg38UCSC Ensembl
chr15:83693799..83694830hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381032
hg191032
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587012
Supporting Variants
Samples
Known GenesBTBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240429
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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