A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070601



Internal ID21450242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48675268..48675327hg38UCSC Ensembl
chr10:49883313..49883372hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594433
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070601
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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