A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3919



Internal ID15191960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3241169..3293917hg38UCSC Ensembl
Outerchr11:3262399..3315147hg19UCSC Ensembl
Outerchr11:3218975..3271723hg18UCSC Ensembl
Outerchr11:3218975..3271723hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3852749
hg1952749
hg1852749
hg1752749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7649
Supporting Variants
SamplesNA12878
Known Genes
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)nssv3919
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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