A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485760



Internal ID22543672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114825874..114831487hg38UCSC Ensembl
chr2:115583451..115589064hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg385614
hg195614
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831180
Supporting Variants
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485760
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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