A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849770



Internal ID22624705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56789815..56823565hg38UCSC Ensembl
chr10:58549575..58583325hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3833751
hg1933751
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849770
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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