A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011437



Internal ID19100654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:189610760..189673312hg38UCSC Ensembl
Innerchr1:189579890..189642442hg19UCSC Ensembl
Innerchr1:187846513..187909065hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3862553
hg1962553
hg1862553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3704854
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)nsv1011437
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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