A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1965n100



Internal ID22788052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97662843..97674343hg38UCSC Ensembl
chr14:98129180..98140680hg19UCSC Ensembl
chr14:97198933..97210433hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3811501
hg1911501
hg1811501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044048, nsv1038300, nsv1044519, nsv1046961, nsv1040240, nsv1050552
Samples
Known GenesLOC100129345
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1965n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss41
Observed Complex0
Frequencyn/a


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