A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578077



Internal ID20951148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25475818..25476491hg38UCSC Ensembl
chr15:25720965..25721638hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38674
hg19674
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578077
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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