A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3908



Internal ID15201878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:89441138..89486316hg38UCSC Ensembl
Outerchr3:89490288..89535466hg19UCSC Ensembl
Outerchr3:89572978..89618156hg18UCSC Ensembl
Outerchr3:89572978..89618156hg17UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3845179
hg1945179
hg1845179
hg1745179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3183, nssv9622
SamplesNA18507, NA12878
Known GenesEPHA3
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv3908
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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