A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407



Internal ID15551313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:134051940..134107192hg38UCSC Ensembl
Outerchr8:135064183..135119435hg19UCSC Ensembl
Outerchr8:135133365..135188617hg18UCSC Ensembl
Outerchr8:135133365..135188617hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3855253
hg1955253
hg1855253
hg1755253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777, nssv11198, nssv3691, nssv6256, nssv5134
SamplesNA12156, NA12878, NA15510, NA19240, NA19129
Known Genes
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)nsv6407
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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