A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862441



Internal ID22637376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99482557..99486425hg38UCSC Ensembl
chr7:99080180..99084048hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383869
hg193869
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504287
Samples
Known GenesZNF789
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862441
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