A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596



Internal ID15551521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86511625..86547281hg38UCSC Ensembl
Outerchr9:89126540..89162196hg19UCSC Ensembl
Outerchr9:88316360..88352016hg18UCSC Ensembl
Outerchr9:86356094..86391750hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3835657
hg1935657
hg1835657
hg1735657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8625
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)nsv6596
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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