A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563503



Internal ID20936574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139070790..139071179hg38UCSC Ensembl
chr7:138755536..138755925hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274402
Samples
Known GenesZC3HAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563503
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