A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612



Internal ID15204853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:91728362..91773456hg38UCSC Ensembl
Outerchr9:94490644..94535738hg19UCSC Ensembl
Outerchr9:93530465..93575559hg18UCSC Ensembl
Outerchr9:91570199..91615293hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3845095
hg1945095
hg1845095
hg1745095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8631
SamplesNA12156
Known GenesROR2
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)nsv6612
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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