A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949772



Internal ID16951959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:3699474..3814873hg38UCSC Ensembl
Outerchr4:3701201..3816600hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38115400
hg19115400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996644
SamplesBILGI_BIOE
Known GenesADRA2C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949772
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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