A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10845



Internal ID15541953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:124877576..124904425hg38UCSC Ensembl
Outerchr11:124747472..124774321hg19UCSC Ensembl
Outerchr11:124252682..124279531hg18UCSC Ensembl
Outerchr11:124252682..124279531hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3812654
hg1912654
hg1812654
hg1712654
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv531
Supporting Variants
SamplesNA18956
Known GenesROBO3, ROBO4
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)nssv10845
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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