A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997569



Internal ID17290521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:169772705..169778804hg38UCSC Ensembl
Outerchr6:170172801..170178900hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv949903
Supporting Variants
SamplesBILGI_BIOE
Known GenesERMARD
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997569
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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