A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002206



Internal ID19091423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108103935..108119014hg38UCSC Ensembl
Innerchr1:108646557..108661636hg19UCSC Ensembl
Innerchr1:108448080..108463159hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3815080
hg1915080
hg1815080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv249n100
Supporting Variantsnssv3484615
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)nsv1002206
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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