A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848708



Internal ID22623643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133088241..133102719hg38UCSC Ensembl
chr7:132773001..132787479hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3814479
hg1914479
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848708
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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