A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735945



Internal ID20511888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25723181..25723308hg38UCSC Ensembl
chr2:25946050..25946177hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270278
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735945
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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