A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17113436



Internal ID21444621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4612586..4612586hg38UCSC Ensembl
chr2:4660176..4660176hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622241
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17113436
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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