A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006716



Internal ID19095934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:209088307..209112437hg38UCSC Ensembl
Innerchr1:209261652..209285782hg19UCSC Ensembl
Innerchr1:207328275..207352405hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3824131
hg1924131
hg1824131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3491613
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)nsv1006716
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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