A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088778



Internal ID21478470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4211497..4211667hg38UCSC Ensembl
chr16:4261498..4261668hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596429
Supporting Variants
SamplesHG03486
Known GenesSRL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088778
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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