A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1949n100



Internal ID22788036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85383797..85432388hg38UCSC Ensembl
chr14:85850141..85898732hg19UCSC Ensembl
chr14:84919894..84968485hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3848592
hg1948592
hg1848592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035826, nsv1041194
Samples
Known GenesLINC00911
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1949n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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