A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863029



Internal ID22637964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102804610..102807138hg38UCSC Ensembl
chr10:104564367..104566895hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg382529
hg192529
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456159
Samples
Known GenesWBP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863029
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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