A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5337



Internal ID15550136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:68865231..68871182hg38UCSC Ensembl
Outerchr6:69575123..69581074hg19UCSC Ensembl
Outerchr6:69631844..69637795hg18UCSC Ensembl
Outerchr6:69631844..69637795hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg385952
hg195952
hg185952
hg175952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8258
SamplesNA12156
Known GenesBAI3
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)nsv5337
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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