A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860607



Internal ID22635542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4724321..4727518hg38UCSC Ensembl
chr10:4766513..4769710hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383198
hg193198
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455268, nssv17453749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860607
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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