A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949803



Internal ID17298677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:16031678..16037877hg38UCSC Ensembl
Outerchr4:16033301..16039500hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996674
SamplesBILGI_BIOE
Known GenesPROM1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949803
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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