A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519



Internal ID15551436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:30410868..30444958hg38UCSC Ensembl
Outerchr9:30410866..30444956hg19UCSC Ensembl
Outerchr9:30400866..30434956hg18UCSC Ensembl
Outerchr9:30400866..30434956hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg385349
hg195349
hg185349
hg175349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8600
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)nsv6519
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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