A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068494



Internal ID21508100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1038970..1039032hg38UCSC Ensembl
chr10:1084910..1084972hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604150
Supporting Variants
SamplesNA20509
Known GenesIDI2-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068494
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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