A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449



Internal ID15203573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:117633483..117678588hg38UCSC Ensembl
Outerchr6:117954646..117999751hg19UCSC Ensembl
Outerchr6:118061339..118106444hg18UCSC Ensembl
Outerchr6:118061339..118106444hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3845106
hg1945106
hg1845106
hg1745106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8286
SamplesNA12156
Known GenesNUS1
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)nsv5449
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer