A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578768



Internal ID20951839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84722922..84724071hg38UCSC Ensembl
chr15:85266153..85267302hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381150
hg191150
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2614n223
Supporting Variantsnssv18240470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578768
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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