A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002787



Internal ID16949053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:3833184..3833261hg38UCSC Ensembl
Outerchr18:3833184..3833261hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954132
Supporting Variants
SamplesBILGI_BIOE
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002787
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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