A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002111



Internal ID19091328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36066685..36105103hg38UCSC Ensembl
Innerchr2:36293828..36332246hg19UCSC Ensembl
Innerchr2:36147332..36185750hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3838419
hg1938419
hg1838419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3789n100
Supporting Variantsnssv3581467
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002111
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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