A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981



Internal ID15198237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1877794..1927695hg38UCSC Ensembl
Outerchr11:1899024..1948925hg19UCSC Ensembl
Outerchr11:1855600..1905501hg18UCSC Ensembl
Outerchr11:1855600..1905501hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3849902
hg1949902
hg1849902
hg1749902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7643
Supporting Variants
SamplesNA19240
Known GenesLSP1, TNNT3
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)nssv981
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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