A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563037



Internal ID20936108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21290258..21291165hg38UCSC Ensembl
chr7:21329876..21330783hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273909
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563037
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