A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6086



Internal ID15191092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:121986190..122034159hg38UCSC Ensembl
Outerchr6:122307336..122355305hg19UCSC Ensembl
Outerchr6:122349035..122397004hg18UCSC Ensembl
Outerchr6:122349035..122397004hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3847970
hg1947970
hg1847970
hg1747970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459
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)nssv6086
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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