A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088186



Internal ID21455507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15514260..15514260hg38UCSC Ensembl
chr17:15417574..15417574hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644800
Supporting Variants
SamplesHG02011
Known GenesTVP23C, TVP23C-CDRT4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088186
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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