A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7678



Internal ID15552711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:11508569..11548052hg38UCSC Ensembl
Outerchr11:11530116..11569599hg19UCSC Ensembl
Outerchr11:11486692..11526175hg18UCSC Ensembl
Outerchr11:11486692..11526175hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3839484
hg1939484
hg1839484
hg1739484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8881
SamplesNA12156
Known GenesGALNT18
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)nsv7678
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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