A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121151



Internal ID19257360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41573815..41577885hg38UCSC Ensembl
Outerchr15:41866013..41870083hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384071
hg194071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1201n106
Supporting Variantsnssv3966273, nssv3964353
SamplesKWS2, KWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121151
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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