A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118070



Internal ID18932781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5887629..5890887hg38UCSC Ensembl
Outerchr10:5929592..5932850hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383259
hg193259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980275
SamplesKWS1
Known GenesANKRD16, FBXO18
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118070
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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