A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2488n100



Internal ID22788575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27672432..27689357hg38UCSC Ensembl
chr15:27917578..27934503hg19UCSC Ensembl
chr15:25591173..25608098hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3816926
hg1916926
hg1816926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048311, nsv1045614, nsv1041642, nsv1037530
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2488n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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