A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1917



Internal ID15194514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1007585..1008768hg38UCSC Ensembl
Outerchr11:1007585..1008768hg19UCSC Ensembl
Outerchr11:997585..998768hg18UCSC Ensembl
Outerchr11:997585..998768hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3810377
hg1910377
hg1810377
hg1710377
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7637
Supporting Variants
SamplesNA18555
Known GenesAP2A2
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)nssv1917
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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