A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17108575



Internal ID21494459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136890474..136890474hg38UCSC Ensembl
chr2:137648044..137648044hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612067
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17108575
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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