A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097562



Internal ID21500364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2345482..2345659hg38UCSC Ensembl
chr16:2395483..2395660hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591485
Supporting Variants
SamplesNA19239
Known GenesABCA17P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097562
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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