A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6089



Internal ID15537774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:133018366..133027907hg38UCSC Ensembl
Outerchr6:133339505..133349046hg19UCSC Ensembl
Outerchr6:133381198..133390739hg18UCSC Ensembl
Outerchr6:133381198..133390739hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg389542
hg199542
hg189542
hg179542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481
Supporting Variants
SamplesNA12156
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)nssv6089
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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