A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3964



Internal ID15548626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:120067776..120112851hg38UCSC Ensembl
Outerchr3:119786623..119831698hg19UCSC Ensembl
Outerchr3:121269313..121314388hg18UCSC Ensembl
Outerchr3:121269313..121314388hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3845076
hg1945076
hg1845076
hg1745076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7853
SamplesNA12156
Known GenesGSK3B
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)nsv3964
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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