A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115619



Internal ID21503819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85545712..85545712hg38UCSC Ensembl
chr2:85772835..85772835hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613225
Supporting Variants
SamplesNA19239
Known GenesGGCX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115619
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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