A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520095



Internal ID21844454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102632104..102632104hg38UCSC Ensembl
chr2:103248563..103248563hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059551
Supporting Variants
Samples
Known GenesSLC9A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520095
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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