A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857699



Internal ID22632634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141149514..141159117hg38UCSC Ensembl
chr8:142159613..142169216hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg389604
hg199604
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507588
Samples
Known GenesDENND3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857699
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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