A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951136



Internal ID17300010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:43708858..43983657hg38UCSC Ensembl
Outerchr8:43564001..43838800hg19UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38274800
hg19274800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999262
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951136
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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