A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464



Internal ID15204690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:5883378..5914698hg38UCSC Ensembl
Outerchr9:5883378..5914698hg19UCSC Ensembl
Outerchr9:5873378..5904698hg18UCSC Ensembl
Outerchr9:5873378..5904698hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg388419
hg198419
hg188419
hg178419
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3703
SamplesNA12878
Known GenesMLANA
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)nsv6464
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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