A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1954n100



Internal ID20153570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87932015..87956225hg38UCSC Ensembl
chr14:88398359..88422569hg19UCSC Ensembl
chr14:87468112..87492322hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3824211
hg1924211
hg1824211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045768, nsv1046684, nsv1036923, nsv1040992, nsv1037168, nsv1038464
Samples
Known GenesGALC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1954n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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