A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2663n100



Internal ID22788750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93598378..93625983hg38UCSC Ensembl
chr15:94141607..94169212hg19UCSC Ensembl
chr15:91942611..91970216hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3827606
hg1927606
hg1827606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041464, nsv1036696, nsv1040193, nsv1043930, nsv1054908, nsv1040431
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)dgv2663n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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