A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956878



Internal ID17305751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:48416492..48416700hg38UCSC Ensembl
Outerchr4:48418509..48418717hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005261
SamplesBILGI_BIOE
Known GenesSLAIN2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956878
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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