A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118013



Internal ID18910077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41573498..41573679hg38UCSC Ensembl
Outerchr15:41865696..41865877hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1200n106
Supporting Variantsnssv3980215
SamplesKWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118013
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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