A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286385



Internal ID20495603
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 StatusS
Merged Variantsnsv4738314
Supporting Variants
Samples
Known GenesITGA4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286385
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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