A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464



Internal ID15550276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:124595592..124640406hg38UCSC Ensembl
Outerchr6:124916738..124961552hg19UCSC Ensembl
Outerchr6:124958437..125003251hg18UCSC Ensembl
Outerchr6:124958437..125003251hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3844815
hg1944815
hg1844815
hg1744815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8293
SamplesNA12156
Known GenesNKAIN2
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)nsv5464
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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