A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409595



Internal ID22467465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:115490352..115493976hg38UCSC Ensembl
chr2:116247928..116251552hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg383625
hg193625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892452
Supporting Variants
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409595
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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