A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581679



Internal ID20954750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96646767..96647578hg38UCSC Ensembl
chr15:97189997..97190808hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38812
hg19812
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581679
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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