A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2842



Internal ID15200719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:98803754..98835494hg38UCSC Ensembl
Outerchr2:99420217..99451957hg19UCSC Ensembl
Outerchr2:98786649..98818389hg18UCSC Ensembl
Outerchr2:98878735..98910475hg17UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg388018
hg198018
hg188018
hg178018
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2283, nssv4443
SamplesNA12878, NA18555
Known GenesKIAA1211L
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)nsv2842
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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