A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4465n54



Internal ID18996641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34412954..34480586hg38UCSC Ensembl
chr15:34705155..34772787hg19UCSC Ensembl
chr15:32492447..32560079hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3867633
hg1967633
hg1867633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568985, nsv568980, nsv568979, nsv568950, nsv568986, nsv568976, nsv568978, nsv568959
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4465n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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