A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057135



Internal ID18799666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..28263325hg38UCSC Ensembl
Innerchr19:27747981..28754232hg19UCSC Ensembl
Innerchr19:32439821..33446072hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg381006253
hg191006252
hg181006252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3501n100
Supporting Variantsnssv3572043
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)nsv1057135
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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