A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572715



Internal ID20945786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75933038..75933405hg38UCSC Ensembl
chr7:75562356..75562723hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276577
Samples
Known GenesPOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572715
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