A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009511



Internal ID19098729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:228656037..228717918hg38UCSC Ensembl
Innerchr1:228791784..228853665hg19UCSC Ensembl
Innerchr1:226858407..226920288hg18UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3861882
hg1961882
hg1861882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3487268
Samples
Known GenesRHOU
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009511
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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