A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6736



Internal ID15551675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:131368366..131412527hg38UCSC Ensembl
Outerchr9:134243753..134287914hg19UCSC Ensembl
Outerchr9:133233574..133277735hg18UCSC Ensembl
Outerchr9:131273307..131317468hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3844162
hg1944162
hg1844162
hg1744162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1804
SamplesNA18555
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)nsv6736
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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