A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862516



Internal ID22637451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6631599..6674506hg38UCSC Ensembl
chr10:6673561..6716468hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3842908
hg1942908
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862516
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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