A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126100



Internal ID19273206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:47428398..47428617hg38UCSC Ensembl
Outerchr15:47720595..47720814hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1207n106
Supporting Variantsnssv3984308
SamplesKWS1
Known GenesSEMA6D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126100
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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