A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996634



Internal ID17289586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:3305374..3311573hg38UCSC Ensembl
Outerchr4:3307101..3313300hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv949762
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996634
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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