A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070616



Internal ID21405022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49069970..49070286hg38UCSC Ensembl
chr10:50278015..50278331hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601490
Supporting Variants
SamplesHG00512
Known GenesVSTM4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070616
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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