A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129940



Internal ID18904860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68421006..68421218hg38UCSC Ensembl
Outerchr15:68713345..68713557hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1232n106
Supporting Variantsnssv3965078
SamplesKWS2
Known GenesITGA11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129940
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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