A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131831



Internal ID18940163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:18594146..18594337hg38UCSC Ensembl
Outerchr8:18451656..18451847hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3788n106
Supporting Variantsnssv3986399
SamplesKWS1
Known GenesPSD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131831
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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