A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587888



Internal ID20960959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66347647..66348395hg38UCSC Ensembl
chr15:66639985..66640733hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238938
Samples
Known GenesTIPIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587888
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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