A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112882



Internal ID18922471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:77210175..77211075hg38UCSC Ensembl
Outerchr5:76506000..76506900hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3099n106
Supporting Variantsnssv3967382
SamplesKWS2
Known GenesPDE8B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112882
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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