A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151822



Internal ID18855466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:94954080..94954164hg38UCSC Ensembl
Outerchr5:94289784..94289868hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999001
SamplesKWB1
Known GenesMCTP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151822
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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