A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950397



Internal ID17299271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:134923411..134928510hg38UCSC Ensembl
Outerchr5:134259101..134264200hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997830
SamplesBILGI_BIOE
Known GenesMIR4461, PCBD2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950397
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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