A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016202



Internal ID22077833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241841181..242092535hg38UCSC Ensembl
Outerchr2:241840119..242095102hg38UCSC Ensembl
Innerchr2:242783333..243034686hg19UCSC Ensembl
Outerchr2:242782271..243037253hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38254984
hg19254983
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155932
Supporting Variants
Samples
Known GenesCXXC11, LOC728323, PDCD1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016202
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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