A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11007



Internal ID15539595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:3175576..3196089hg38UCSC Ensembl
Outerchr2:3179347..3199860hg19UCSC Ensembl
Outerchr2:3158354..3178867hg18UCSC Ensembl
Outerchr2:4717630..4738143hg17UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg389854
hg199854
hg189854
hg179854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2581
Supporting Variants
SamplesNA15510
Known GenesTSSC1
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)nssv11007
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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