A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145068



Internal ID19277188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:93584094..93585194hg38UCSC Ensembl
Outerchr5:92919800..92920900hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3128n106
Supporting Variantsnssv3981687
SamplesKWS1
Known GenesNR2F1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145068
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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