A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738314



Internal ID20514282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181491251..181491566hg38UCSC Ensembl
chr2:182355978..182356293hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286385
Samples
Known GenesITGA4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738314
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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