A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577247



Internal ID20950318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78366629..78367825hg38UCSC Ensembl
chr15:78658971..78660167hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2599n223
Supporting Variantsnssv18239720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577247
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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