A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289604



Internal ID20498822
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 StatusS
Merged Variantsnsv4737534
Supporting Variants
Samples
Known GenesSLC9A4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289604
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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