A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842851



Internal ID22617786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67734645..67735751hg38UCSC Ensembl
chr5:67030473..67031579hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg381107
hg191107
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842851
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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