A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4626



Internal ID15543334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:58683571..58710817hg38UCSC Ensembl
Outerchr11:58451044..58478290hg19UCSC Ensembl
Outerchr11:58207620..58234866hg18UCSC Ensembl
Outerchr11:58207620..58234866hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3827247
hg1927247
hg1827247
hg1727247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv329
Supporting Variants
SamplesNA19129
Known GenesGLYAT
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)nssv4626
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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