A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4702n54



Internal ID22772597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87245241..87334019hg38UCSC Ensembl
chr15:87788472..87877250hg19UCSC Ensembl
chr15:85589476..85678254hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3888779
hg1988779
hg1888779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570363, nsv570364, nsv570360, nsv570362, nsv570361
SamplesNINDS_260, NINDS_186, NINDS_258
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4702n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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