A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4690n54



Internal ID22772585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84869224..84919085hg38UCSC Ensembl
chr15:85412455..85462316hg19UCSC Ensembl
chr15:83213459..83263320hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3849862
hg1949862
hg1849862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570287, nsv570288
SamplesHGDP00562, HGDP00564
Known GenesALPK3, SLC28A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4690n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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