A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002307



Internal ID19091524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11405410..11467498hg38UCSC Ensembl
Innerchr1:11465467..11527555hg19UCSC Ensembl
Innerchr1:11388054..11450142hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3862089
hg1962089
hg1862089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3481323
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)nsv1002307
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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