A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4419n54



Internal ID20137843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30194842..30537608hg38UCSC Ensembl
chr15:30487045..30829811hg19UCSC Ensembl
chr15:28274337..28617103hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38342767
hg19342767
hg18342767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568735, nsv568730, nsv568724, nsv568723, nsv568737, nsv568726
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4419n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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