A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860270



Internal ID22635205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18554812..18625262hg38UCSC Ensembl
chr10:18843741..18914191hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3870451
hg1970451
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452379
Samples
Known GenesNSUN6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860270
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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