A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846925



Internal ID22621860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3151981..3169500hg38UCSC Ensembl
chr7:3191614..3209133hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3817520
hg1917520
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505480, nssv17505479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846925
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