A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864233



Internal ID22639168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111072017..111085729hg38UCSC Ensembl
chr7:110712073..110725785hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3813713
hg1913713
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500670
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864233
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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