A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4141n106



Internal ID20163498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127870800..127871836hg38UCSC Ensembl
chr9:130633079..130634115hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381037
hg191037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1114775, nsv1117755
SamplesKWS1
Known GenesAK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4141n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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