A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950395



Internal ID17299269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:132819009..132833008hg38UCSC Ensembl
Outerchr5:132154701..132168700hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3814000
hg1914000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997828
SamplesBILGI_BIOE
Known GenesSHROOM1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950395
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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