A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950093



Internal ID17298967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:76542476..76549775hg38UCSC Ensembl
Outerchr5:75838301..75845600hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997782
SamplesBILGI_BIOE
Known GenesIQGAP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950093
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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