A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111509



Internal ID18934994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:40037595..40037719hg38UCSC Ensembl
Outerchr15:40329796..40329920hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1193n106
Supporting Variantsnssv3963645
SamplesKWS2
Known GenesSRP14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111509
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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