A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11108



Internal ID15539600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:155266014..155271888hg38UCSC Ensembl
Outerchr1:155235805..155241679hg19UCSC Ensembl
Outerchr1:153502429..153508303hg18UCSC Ensembl
Outerchr1:152048878..152054752hg17UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3831468
hg1931468
hg1831468
hg1731468
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3010
Supporting Variants
SamplesNA15510
Known GenesCLK2
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)nssv11108
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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