A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1117994



Internal ID19258023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41559396..41561150hg38UCSC Ensembl
Outerchr15:41851594..41853348hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381755
hg191755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1194n106
Supporting Variantsnssv3980196
SamplesKWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1117994
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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