A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008011



Internal ID19097230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88932272..89284138hg38UCSC Ensembl
Innerchr2:89231790..89583895hg19UCSC Ensembl
Innerchr2:89012905..89365010hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38351867
hg19352106
hg18352106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3933n100
Supporting Variantsnssv3729985
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)nsv1008011
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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