A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867136



Internal ID22642071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91263124..91265365hg38UCSC Ensembl
chr7:90892439..90894680hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg382242
hg192242
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504193
Samples
Known GenesFZD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867136
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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