A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3922



Internal ID15538649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:4925104..4958143hg38UCSC Ensembl
Outerchr11:4946334..4979373hg19UCSC Ensembl
Outerchr11:4902910..4935949hg18UCSC Ensembl
Outerchr11:4902910..4935949hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3833040
hg1933040
hg1833040
hg1733040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7652
Supporting Variants
SamplesNA12878
Known GenesOR51A2, OR51A4
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)nssv3922
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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