A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950488



Internal ID16952675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:106513426..106548125hg38UCSC Ensembl
Outerchr6:106961301..106996000hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3834700
hg1934700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997499
SamplesBILGI_BIOE
Known GenesAIM1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950488
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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