A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576032



Internal ID20949103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82987168..82988059hg38UCSC Ensembl
chr15:83655920..83656811hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240425
Samples
Known GenesFAM103A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576032
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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