A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737534



Internal ID20513495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102492657..102492745hg38UCSC Ensembl
chr2:103109116..103109204hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289604
Samples
Known GenesSLC9A4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737534
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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