A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5167



Internal ID15203263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:442174..486632hg38UCSC Ensembl
Outerchr6:442174..486632hg19UCSC Ensembl
Outerchr6:387174..431632hg18UCSC Ensembl
Outerchr6:387174..431632hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3844459
hg1944459
hg1844459
hg1744459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2567
SamplesNA18555
Known GenesEXOC2
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)nsv5167
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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