A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613325



Internal ID21561630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64612210..64612210hg38UCSC Ensembl
chr2:64839344..64839344hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114762
SamplesHG00733
Known GenesLOC339807
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613325
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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