A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458



Internal ID15550269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:121466375..121501908hg38UCSC Ensembl
Outerchr6:121787521..121823054hg19UCSC Ensembl
Outerchr6:121829220..121864753hg18UCSC Ensembl
Outerchr6:121829220..121864753hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3835534
hg1935534
hg1835534
hg1735534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4607
SamplesNA19129
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)nsv5458
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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