A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958479



Internal ID17307352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:107361576..107361655hg38UCSC Ensembl
Outerchr8:108373804..108373883hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001197
SamplesBILGI_BIOE
Known GenesANGPT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958479
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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