A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856944



Internal ID22631879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100476416..100477644hg38UCSC Ensembl
chr10:102236173..102237401hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg381229
hg191229
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458013
Samples
Known GenesWNT8B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856944
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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