A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3003533



Internal ID16949799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:501478..501544hg38UCSC Ensembl
Outerchr6:501478..501544hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955934
Supporting Variants
SamplesBILGI_BIOE
Known GenesEXOC2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3003533
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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