A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866946



Internal ID22641881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148889670..148891599hg38UCSC Ensembl
chr7:148586762..148588691hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381930
hg191930
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502620
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866946
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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