A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060674



Internal ID18803205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27809088hg38UCSC Ensembl
Innerchr19:27747981..28299996hg19UCSC Ensembl
Innerchr19:32439821..32991836hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38552016
hg19552016
hg18552016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3500n100
Supporting Variantsnssv3572040
Samples
Known GenesLINC00662
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060674
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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