A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2666n100



Internal ID22788753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97347055..97393999hg38UCSC Ensembl
chr15:97890285..97937229hg19UCSC Ensembl
chr15:95691289..95738233hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3846945
hg1946945
hg1846945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043053, nsv1051209
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)dgv2666n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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