A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849212



Internal ID22624147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21563868..21567167hg38UCSC Ensembl
chr10:21852797..21856096hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450148
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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