A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2844



Internal ID15547407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:98977599..99022298hg38UCSC Ensembl
Outerchr2:99594062..99638761hg19UCSC Ensembl
Outerchr2:98960494..99005193hg18UCSC Ensembl
Outerchr2:99052580..99097279hg17UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3844700
hg1944700
hg1844700
hg1744700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5809
SamplesNA19129
Known GenesTSGA10
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)nsv2844
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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