A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607570



Internal ID21555875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37903655..37903655hg38UCSC Ensembl
chr2:38130798..38130798hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113148
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607570
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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