A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088614



Internal ID21455142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28279225..28279225hg38UCSC Ensembl
chr17:26606251..26606251hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654273
Supporting Variants
SamplesHG02011
Known GenesKRT18P55
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088614
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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