A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2825



Internal ID15547388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:89896119..89968953hg38UCSC Ensembl
Outerchr2:89934929..90007763hg19UCSC Ensembl
Outerchr2:89571971..89645064hg18UCSC Ensembl
Outerchr2:89630118..89703211hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3872835
hg1972835
hg1873094
hg1773094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6857
SamplesNA12156
Known Genes
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)nsv2825
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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