A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1925



Internal ID15541208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:4825578..4858784hg38UCSC Ensembl
Outerchr11:4846808..4880014hg19UCSC Ensembl
Outerchr11:4803384..4836590hg18UCSC Ensembl
Outerchr11:4803384..4836590hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386802
hg196802
hg186802
hg176802
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7651
Supporting Variants
SamplesNA18555
Known GenesOR51S1
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)nssv1925
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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