A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5169



Internal ID15203265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:652308..681630hg38UCSC Ensembl
Outerchr6:652308..681630hg19UCSC Ensembl
Outerchr6:597308..626630hg18UCSC Ensembl
Outerchr6:597308..626630hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3829323
hg1929323
hg1829323
hg1729323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2568
SamplesNA18555
Known GenesEXOC2, HUS1B
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)nsv5169
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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