A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512



Internal ID15551429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:27155679..27200457hg38UCSC Ensembl
Outerchr9:27155677..27200455hg19UCSC Ensembl
Outerchr9:27145677..27190455hg18UCSC Ensembl
Outerchr9:27145677..27190455hg17UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3844779
hg1944779
hg1844779
hg1744779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8597
SamplesNA12156
Known GenesTEK
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)nsv6512
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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