A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950174



Internal ID17299048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:44684864..44701363hg38UCSC Ensembl
Outerchr6:44652601..44669100hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3816500
hg1916500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997445
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950174
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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