A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485768



Internal ID22543680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:115490377..115494158hg38UCSC Ensembl
chr2:116247953..116251734hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg383782
hg193782
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830907
Supporting Variants
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485768
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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