A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950559



Internal ID17299433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:24557078..24572577hg38UCSC Ensembl
Outerchr4:24558701..24574200hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3815500
hg1915500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996685
SamplesBILGI_BIOE
Known GenesDHX15
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950559
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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