A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2885



Internal ID15547448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:114889807..114935433hg38UCSC Ensembl
Outerchr2:115647384..115693010hg19UCSC Ensembl
Outerchr2:115363854..115409480hg18UCSC Ensembl
Outerchr2:115363614..115409240hg17UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3845627
hg1945627
hg1845627
hg1745627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6865
SamplesNA12156
Known GenesDPP10
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)nsv2885
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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