A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014959



Internal ID19104176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:117490138..117641566hg38UCSC Ensembl
Innerchr2:118247714..118399142hg19UCSC Ensembl
Innerchr2:117964184..118115612hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38151429
hg19151429
hg18151429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4060n100
Supporting Variantsnssv3580683
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)nsv1014959
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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