A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833846



Internal ID6159570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:45884263..45972347hg19UCSC Ensembl
Outerchr19:50576103..50664187hg18UCSC Ensembl
Outerchr19:50576103..50664187hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1454752
Samples
Known GenesCD3EAP, ERCC1, FOSB, PPP1R13L
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833846
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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