A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998907



Internal ID16945173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79748501..79756200hg38UCSC Ensembl
Outerchr18:77508501..77516200hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953928
Supporting Variants
SamplesBILGI_BIOE
Known GenesCTDP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998907
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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