A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118330



Internal ID18901836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:83284348..83284848hg38UCSC Ensembl
Outerchr15:83953100..83953600hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1257n106
Supporting Variantsnssv3981008
SamplesKWS1
Known GenesBNC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118330
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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