A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585779



Internal ID21534327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6816579..6816628hg38UCSC Ensembl
chr10:6858541..6858590hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070896
SamplesHG01505
Known GenesLINC00707
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585779
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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