A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17114441



Internal ID21458631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5405054..5405054hg38UCSC Ensembl
chr2:5545187..5545187hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613920
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17114441
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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