A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863430



Internal ID22638365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8654356..8657942hg38UCSC Ensembl
chr10:8696319..8699905hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383587
hg193587
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863430
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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