A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2615n100



Internal ID20154231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68083566..68144258hg38UCSC Ensembl
chr15:68375904..68436596hg19UCSC Ensembl
chr15:66162958..66223650hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3860693
hg1960693
hg1860693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049860, nsv1050541
Samples
Known GenesPIAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2615n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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