A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2614n100



Internal ID22788701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61392006..61408370hg38UCSC Ensembl
chr15:61684205..61700569hg19UCSC Ensembl
chr15:59471497..59487861hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3816365
hg1916365
hg1816365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046354, nsv1042261
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)dgv2614n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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