A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999355



Internal ID16945621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:144236298..144262997hg38UCSC Ensembl
Outerchr8:145291201..145317900hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3826700
hg1926700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950822
Supporting Variants
SamplesBILGI_BIOE
Known GenesMIR7112-2, MROH1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999355
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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