A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533



Internal ID15551452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:37080633..37113289hg38UCSC Ensembl
Outerchr9:37080630..37113286hg19UCSC Ensembl
Outerchr9:37070630..37103286hg18UCSC Ensembl
Outerchr9:37070630..37103286hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg388343
hg198343
hg188343
hg178343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv798
SamplesNA19240
Known GenesLOC100506710
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)nsv6533
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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