A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999295



Internal ID16945561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:70135766..70154565hg38UCSC Ensembl
Outerchr8:71048001..71066800hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3818800
hg1918800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951442
Supporting Variants
SamplesBILGI_BIOE
Known GenesNCOA2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999295
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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