A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110067



Internal ID21458547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216261661..216261661hg38UCSC Ensembl
chr2:217126384..217126384hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621077
Supporting Variants
SamplesHG02587
Known GenesMARCH4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110067
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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