A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055913



Internal ID18798444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6267599..6327675hg38UCSC Ensembl
Innerchr19:6267610..6327686hg19UCSC Ensembl
Innerchr19:6218610..6278686hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3860077
hg1960077
hg1860077
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564612
Samples
Known GenesACER1, MLLT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055913
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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