A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061090



Internal ID18803621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..28192022hg38UCSC Ensembl
Innerchr19:27747981..28682929hg19UCSC Ensembl
Innerchr19:32439821..33374769hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38934950
hg19934949
hg18934949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3501n100
Supporting Variantsnssv3572042
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)nsv1061090
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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