A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848720



Internal ID22623655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155617446..155621997hg38UCSC Ensembl
chr7:155410140..155414691hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384552
hg194552
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848720
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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