A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155932



Internal ID22086437
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv177n97
Supporting Variantsnssv4016202
Samples
Known GenesCXXC11, LOC728323, PDCD1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155932
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer