A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591197



Internal ID20964268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43853195..43853899hg38UCSC Ensembl
chr15:44145393..44146097hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240198
Samples
Known GenesWDR76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591197
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer