A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067400



Internal ID21490882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1009270..1009270hg38UCSC Ensembl
chr10:1055210..1055210hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625015
Supporting Variants
SamplesNA19238
Known GenesGTPBP4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067400
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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