A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743665



Internal ID20519654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10200392..10200575hg38UCSC Ensembl
chr2:10340518..10340701hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263672
Samples
Known GenesC2orf48
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743665
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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