A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095599



Internal ID21488593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28172116..28172116hg38UCSC Ensembl
chr17:26499142..26499142hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662715
Supporting Variants
SamplesNA18939
Known GenesNLK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095599
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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