A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4181n106



Internal ID20163538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137818548..137819648hg38UCSC Ensembl
chr9:140713000..140714100hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135386, nsv1135298
SamplesKWS2
Known GenesEHMT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4181n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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