A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531



Internal ID15204764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:36832805..36876608hg38UCSC Ensembl
Outerchr9:36832802..36876605hg19UCSC Ensembl
Outerchr9:36822802..36866605hg18UCSC Ensembl
Outerchr9:36822802..36866605hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3843804
hg1943804
hg1843804
hg1743804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8605
SamplesNA12156
Known GenesMIR4540, PAX5
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)nsv6531
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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