A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950674



Internal ID17299548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:43066699..43073598hg38UCSC Ensembl
Outerchr5:43066801..43073700hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997728
SamplesBILGI_BIOE
Known GenesLOC100132356, LOC100506639, LOC648987
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950674
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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