A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059366



Internal ID18801897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27923726hg38UCSC Ensembl
Innerchr19:27747981..28414634hg19UCSC Ensembl
Innerchr19:32439821..33106474hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38666654
hg19666654
hg18666654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3500n100
Supporting Variantsnssv3572041
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)nsv1059366
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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