A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008189



Internal ID19097408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:189906844..189957453hg38UCSC Ensembl
Innerchr1:189875974..189926583hg19UCSC Ensembl
Innerchr1:188142597..188193206hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3850610
hg1950610
hg1850610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3704859
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)nsv1008189
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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