A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102531



Internal ID21290809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36441142..36442464hg38UCSC Ensembl
Innerchr2:36668285..36669607hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118185
Supporting Variants
Samplessample64
Known GenesCRIM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102531
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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