A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5168



Internal ID15203264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:593773..607812hg38UCSC Ensembl
Outerchr6:593773..607812hg19UCSC Ensembl
Outerchr6:538773..552812hg18UCSC Ensembl
Outerchr6:538773..552812hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3814040
hg1914040
hg1814040
hg1714040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8208
SamplesNA12156
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)nsv5168
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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