A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071597



Internal ID21484976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:700326..700457hg38UCSC Ensembl
chr10:746266..746397hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591385
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071597
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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