A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070896



Internal ID21451413
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 StatusS
Merged Variantsnsv5585779
Supporting Variants
SamplesHG01505
Known GenesLINC00707
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070896
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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