A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846899



Internal ID22621834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24727923..24730272hg38UCSC Ensembl
chr7:24767542..24769891hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382350
hg192350
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1851n209
Supporting Variantsnssv17504791, nssv17504790
Samples
Known GenesDFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846899
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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