A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138391



Internal ID19255399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:78632191..78632253hg38UCSC Ensembl
Outerchr15:78924533..78924595hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1249n106
Supporting Variantsnssv3990957
SamplesKWS2
Known GenesCHRNB4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138391
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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