A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000230



Internal ID16946496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:4634806..4644105hg38UCSC Ensembl
Outerchr17:4538101..4547400hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952111
Supporting Variants
SamplesBILGI_BIOE
Known GenesALOX15
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000230
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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