A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950493



Internal ID16952680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:109442398..109456197hg38UCSC Ensembl
Outerchr6:109763601..109777400hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3813800
hg1913800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997504
SamplesBILGI_BIOE
Known GenesMICAL1, SMPD2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950493
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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