A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2065



Internal ID15546628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:98753047..98797737hg38UCSC Ensembl
Outerchr1:99218603..99263293hg19UCSC Ensembl
Outerchr1:98991191..99035881hg18UCSC Ensembl
Outerchr1:98930624..98975314hg17UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3844691
hg1944691
hg1844691
hg1744691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7398
SamplesNA12156
Known GenesSNX7
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)nsv2065
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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