A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745777



Internal ID20521787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2786349..2786404hg38UCSC Ensembl
chr2:2790121..2790176hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745777
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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