A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv438n106



Internal ID20159795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44927747..44928702hg38UCSC Ensembl
chr10:45423195..45424150hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38956
hg19956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1131636, nsv1120536
SamplesKWS1
Known GenesTMEM72, TMEM72-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv438n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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