A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1102n106



Internal ID20160459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73529796..73558496hg38UCSC Ensembl
chr14:73996500..74025200hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3828701
hg1928701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121875, nsv1118282
SamplesKWS1, KWS2
Known GenesACOT1, HEATR4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1102n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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