A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096348



Internal ID21492526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16127228..16127313hg38UCSC Ensembl
chr17:16030542..16030627hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603057
Supporting Variants
SamplesNA19238
Known GenesNCOR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096348
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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