A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070330



Internal ID21510743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29629592..29630061hg38UCSC Ensembl
chr10:29918521..29918990hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585763
Supporting Variants
SamplesNA24385
Known GenesSVIL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070330
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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