A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11010



Internal ID15539598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:36104606..36121286hg38UCSC Ensembl
Outerchr2:36331749..36348429hg19UCSC Ensembl
Outerchr2:36185253..36201933hg18UCSC Ensembl
Outerchr2:36243400..36260080hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3816681
hg1916681
hg1816681
hg1716681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2679
Supporting Variants
SamplesNA15510
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)nssv11010
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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