A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7671



Internal ID15206018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9490020..9521570hg38UCSC Ensembl
Outerchr11:9511567..9543117hg19UCSC Ensembl
Outerchr11:9468143..9499693hg18UCSC Ensembl
Outerchr11:9468143..9499693hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387733
hg197733
hg187733
hg177733
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5349
SamplesNA19129
Known GenesZNF143
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)nsv7671
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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