A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6460n54



Internal ID18998636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42400086..42402589hg38UCSC Ensembl
chr19:42904238..42906741hg19UCSC Ensembl
chr19:47596078..47598581hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382504
hg192504
hg182504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579630, nsv579631
Samples
Known GenesLIPE, LIPE-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6460n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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