A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576662



Internal ID20949733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45329054..45329628hg38UCSC Ensembl
chr15:45621252..45621826hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576662
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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