A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5552



Internal ID15550373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:155130475..155175229hg38UCSC Ensembl
Outerchr6:155451609..155496363hg19UCSC Ensembl
Outerchr6:155493301..155538055hg18UCSC Ensembl
Outerchr6:155543722..155588476hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3844755
hg1944755
hg1844755
hg1744755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8317
SamplesNA12156
Known GenesTIAM2
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)nsv5552
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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