A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1200n106



Internal ID20160557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41573466..41573712hg38UCSC Ensembl
chr15:41865664..41865910hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135456, nsv1121509, nsv1118013
SamplesKWS2, KWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1200n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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