A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586041



Internal ID20959112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34072327..34073038hg38UCSC Ensembl
chr15:34364528..34365239hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239530
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586041
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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