A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7059



Internal ID15190119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:151298648..151329483hg38UCSC Ensembl
Outerchr1:151271124..151301959hg19UCSC Ensembl
Outerchr1:149537748..149568583hg18UCSC Ensembl
Outerchr1:148084197..148115032hg17UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg388602
hg198602
hg188602
hg178602
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2821
Supporting Variants
SamplesNA12156
Known GenesPI4KB
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)nssv7059
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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