A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835107



Internal ID22610042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170947487..170954221hg38UCSC Ensembl
chr3:170665276..170672010hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg386735
hg196735
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835107
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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