A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954431



Internal ID16956618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:2961210..2961313hg38UCSC Ensembl
Outerchr4:2962937..2963040hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001962
SamplesBILGI_BIOE
Known GenesNOP14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954431
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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